Pharmacovigilance Scientist
Remote job
Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at ************** and follow us on LinkedIn and X.
About This Role
Axsome Therapeutics is seeking a Pharmacovigilance Scientist to establish and execute pharmacovigilance (PV) systems and procedures, with a strong focus on maintaining high-quality standards. This role is responsible for supporting the Pharmacovigilance (PV) Science function under the guidance of the PV physician and providing oversight of ICSR assessment, signal detection, medical surveillance and risk management activities for investigational products in clinical development and marketed products. This position collaborates with key internal stakeholders, including Clinical Development, Commercial, Medical Information, Medical Affairs, Quality, Regulatory and Legal, as well as multiple external Service Providers and partners on pharmacovigilance-related matters.
This position reports to Executive Director of Pharmacovigilance/Drug Safety and is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles.
Job Responsibilities and Duties include, but are not limited to, the following:
Assist safety physician to enhance safety surveillance and signal detection by monitoring and analyzing safety data from various sources to identify potential safety signals or trends related to investigational and marketed products
Contribute to the creation and execution of risk minimization measures to mitigate identified risks.
Support the preparation pharmacovigilance aggregate safety reports (e.g., PADER, PSURs, DSURs) to regulatory authorities to meet compliance requirements.
Collaborate with PV physician/PV operations and key stakeholders to request/receive applicable sections of the report
Provide training and guidance to other functions to address ad hoc questions and issues
Ensure timely finalization of the reports to meet the submission timelines of relevant health authorities and other external stakeholders
Collaborate and communicate with cross-functional teams to ensure effective safety monitoring and communication
Support the safety review team (SRT) and coordinates all safety topic discussion and documentation.
Ensure appropriate stakeholder representation and input at SRT
Ensure all data is appropriately compiled and presented at SRT for team review
Liaise with SRT chair to facilitate communication and support for decisions resulting from the SRT (e.g. update of RMPs, labeling, regulatory notifications etc.)
Contribute to clinical trials by providing safety input and reviewing documents such as Clinical Study Reports (CSRs), protocols, and investigator brochures (IB), ICF etc.
Provide support for the processing of individual case safety reports (ICSRs) and ensure data accuracy and completeness for investigational and marketed products
Support the PV SOP updates
Oversee vendor safety process, e.g., signal detection, validation and assessment.
Participate in audit/inspection preparedness activities and provide support during regulatory inspections in collaboration with team members
Participate in new study initiation to ensure PV requirements are met including but not limited to safety reporting, query resolution, SAR reconciliation, un-blinding process, and safety reporting training
Evaluate and improve current PV processes, as needed, to strengthen medical surveillance and risk management process ensuring alignment with best practices
Requirements / Qualifications
Master's degree in health-discipline or equivalent required, RN, R.Ph, or Pharm D degree is highly preferred
5+ years of progressively responsible Pharmacovigilance experience in a pharmaceutical, biotechnology, or related environment with focused experience in signal detection, safety surveillance, risk mitigation and risk management
Extensive experience in case processing, regulatory requirements of ICSRs, MedDRA, WHODD, project management
Experience in submission activities in both FDA and EU is preferred, but not required
Must demonstrate the ability to draft reports, business correspondence, and procedures, and to effectively present information and respond to questions from internal and external stakeholders, both domestic and international
Ability to work on site Monday, Tuesday & Thursday. We are unable to consider candidates who are looking for fully remote roles.
Experience and Knowledge
Knowledge of ICH E2B(R2) and (R3) specifications and entry guidance.
Knowledge of global pharmacovigilance reporting rules and timelines, including but not limited to Health Canada, FDA and EMA.
Knowledge of relevant food and drug administration (FDA), European union (EU) and international conference on Harmonization (ICH) guidelines, initiatives, and regulations governing pharmacovigilance.
Ability to interpret health and medical records such as adverse event reporting forms, a discharge summary, etc.
Experience with clinical and/or post-marketing case assessment, including medical terminologies, MedDRA and WHO DD coding and narrative writing.
Experience with safety database is required; ARISg is a plus but not mandatory.
Experience with Veeva is a plus but not mandatory.
Ability to work independently and collaboratively, as required, in a fast-paced matrixed team environment consisting of internal and external team members
Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines
Ability to read, analyze, and interpret professional journals, technical procedures, and governmental regulations
Excellent planning, organization, and time management skills including the ability to support and prioritize multiple projects
Excellent verbal and written communication and skills
Excellent in detailed-oriented tasks.
Salary & Benefits
The anticipated salary range for this role is $150,000 - $185,000. We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities. The salary offer will be based on a variety of factors, including experience, qualifications, internal equity and location. Axsome offers a competitive employment package that includes an annual bonus, significant equity and a generous benefits package.
Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, sexual orientation, gender identity, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law.
Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members. Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration.
Auto-ApplyMachine Learning Scientist III, Recommendations
Remote job
About this role We are looking for an experienced Machine Learning Scientist III to join our content recommendations team. In this role, you will be at the core of building and optimizing ML-based recommender systems (e.g., image and content recommendations, homepage and email optimization and personalization) to enhance the customer experience at Wayfair. Your work will directly impact how millions of customers discover and engage with products, driving significant business value.
As part of Wayfair's SMART (Search, Marketing, and Recommendations Technology) team, you will collaborate with ML scientists, engineers, and product teams to develop and deploy cutting-edge recommendation models that operate at scale. This role is an opportunity to solve complex problems related to personalization, large-scale machine learning, latency, and scalability while leveraging state-of-the-art (SOTA) AI techniques.
What you'll do
* Develop and optimize recommendation models that power personalized experiences across Wayfair's site, app, email, and push notifications.
* Conduct applied research to improve recommender systems using traditional ML techniques, deep learning and reinforcement learning.
* Build scalable ML pipelines for training, evaluation, and inference, ensuring models operate efficiently in production.
* Work closely with engineering teams to deploy models in a production environment, addressing real-world constraints such as latency, interpretability, and scalability.
* Analyze model performance and iterate based on A/B test results, offline evaluation metrics, and business impact.
* Leverage and contribute to open-source ML frameworks while staying up to date with cutting-edge research in recommendation systems.
* Drive innovation by identifying opportunities to improve personalization strategies and developing novel algorithms that enhance customer engagement.
* Collaborate with cross-functional teams including product managers, software engineers, and data scientists to align ML objectives with business goals.
* Mentor other less experienced scientists on the team
Who you are
* 5+ years of experience developing and deploying machine learning models, with a focus on recommendations, ranking, or personalization.
* Strong theoretical understanding of machine learning and deep learning applied to large-scale recommendation problems.
* Experience in training, evaluating, and optimizing recommendation models in production, leveraging techniques such as collaborative filtering, sequence modeling, representation learning and multi-armed bandits.
* Proficiency in Python and experience with ML frameworks such as TensorFlow, PyTorch, or Scikit-Learn.
* Familiarity with big data processing (Spark, Hadoop) and ML pipeline orchestration (Airflow, Kubeflow, MLflow).
* Strong coding skills and familiarity with building scalable ML systems in cloud environments (AWS, GCP, Azure).
* Ability to design experiments and analyze results using A/B testing and statistical techniques.
* Excellent communication skills, with the ability to explain complex ML concepts to non-technical stakeholders and drive data-driven decisions.
Nice to have
* Experience developing core recommendation systems for eCommerce, marketplaces, or streaming platforms.
* Familiarity with reinforcement learning or contextual bandits for adaptive recommendation strategies.
This role offers the opportunity to work on high-impact ML problems at scale, shaping the future of personalization and recommendations at Wayfair. If you're passionate about building intelligent systems that enhance customer experiences, we'd love to hear from you!
Why You'll Love Wayfair:
* Time Off:
* Paid Holidays
* Paid Time Off (PTO)
* Health & Wellness:
* Full Health Benefits (Medical, Dental, Vision, HSA/FSA)
* Life Insurance
* Disability Protection (Short Term & Long Term Disability)
* Global Wellbeing: Gym/Fitness discounts (including US Peloton, Global ClassPass, and various regional gym memberships)
* Mental Health Support (Global Mental Health, Global Wayhealthy Recordings)
* Caregiver Services
* Financial Growth & Security:
* 401K Matching (Employee Matching Program)
* Tuition Reimbursement
* Financial Health Education (Knowledge of Financial Education - KOFE)
* Tax Advantaged Accounts
* Family Support:
* Family Planning Support
* Parental Leave
* Global Surrogacy & Adoption Policy
* Professional Development & Recognition:
* Rewards & Recognition
* Global Employee Anniversary Awards
* Paid Volunteer Work
* Unique Perks:
* Employee Discount
* U.S. Bluebikes Membership
* Global Pod Outings
* Work/Life Balance:
* Emphasizing a supportive & flexible work environment that encourages a balance between personal and professional commitments
Wayfair's In-Office Policy:
All Mountain View-based interns, co-ops, and corporate employees will be in office in a hybrid capacity. Employees will work in the office on designated days, Tuesday, Wednesday, and Thursday, and work remotely the other 2 days of the week.
Assistance for Individuals with Disabilities
Wayfair is fully committed to providing equal opportunities for all individuals, including individuals with disabilities. As part of this commitment, Wayfair will make reasonable accommodations to the known physical or mental limitations of qualified individuals with disabilities, unless doing so would impose an undue hardship on business operations. If you require a reasonable accommodation to participate in the job application or interview process, please let us know by completing our Accomodations for Applicants form.
Need Technical Assistance?
For more information about applying for a career at wayfair, visit our FAQ page here.
About Wayfair Inc.
Wayfair is one of the world's largest online destinations for the home. Whether you work in our global headquarters in Boston, or in our warehouses or offices throughout the world, we're reinventing the way people shop for their homes. Through our commitment to industry-leading technology and creative problem-solving, we are confident that Wayfair will be home to the most rewarding work of your career. If you're looking for rapid growth, constant learning, and dynamic challenges, then you'll find that amazing career opportunities are knocking.
No matter who you are, Wayfair is a place you can call home. We're a community of innovators, risk-takers, and trailblazers who celebrate our differences, and know that our unique perspectives make us stronger, smarter, and well-positioned for success. We value and rely on the collective voices of our employees, customers, community, and suppliers to help guide us as we build a better Wayfair - and world - for all. Every voice, every perspective matters. That's why we're proud to be an equal opportunity employer. We do not discriminate on the basis of race, color, ethnicity, ancestry, religion, sex, national origin, sexual orientation, age, citizenship status, marital status, disability, gender identity, gender expression, veteran status, genetic information, or any other legally protected characteristic.
Your personal data is processed in accordance with our Candidate Privacy Notice (***************************************** If you have any questions or wish to exercise your rights under applicable privacy and data protection laws, please contact us at *********************************.
Easy ApplyApplied Scientist
Remote job
About the company:
The mining industry has steadily become worse at finding new ore deposits, requiring >10X more capital to make discoveries compared to 30 years ago. The easy-to-find, near-surface deposits have largely been found, and the industry has chronically under-invested in new exploration technology, relying on the manual techniques of yesteryear - even as demand accelerates for copper, lithium, and other metals to build electric vehicles, renewable energy, and data centers.
KoBold builds AI models for mineral exploration and deploys those models-alongside our novel sensors-to guide decisions on KoBold-owned-and-operated exploration programs. In the six years since founding, KoBold has become by far both the largest independent mineral exploration company and the largest exploration technology developer. Our data scientists and software engineers, who come from leading technology companies, jointly lead exploration programs with our renowned exploration geologists.
KoBold has proven its first discovery with materially less capital than the industry average and found one of the best copper deposits ever discovered: the copper is far more concentrated than the global average of copper mines, and this asset alone is expected to generate meaningful revenue for decades. KoBold has a portfolio of more than 60 other projects, each of which has the potential for another high-quality discovery.
KoBold is privately held; investors include institutional asset managers T. Rowe Rice and Canada Pension Plan Investments; technology venture capitalists Andreessen Horowitz, Breakthrough Energy Ventures, BOND Capital, and Standard Investments; and natural resources companies Equinor, BHP, and Mitsubishi.
About The Role:
In this role, you will develop state of the art instruments to collect data to guide our exploration programs. You will simulate, characterize, and calibrate sensor performance and design new data acquisition systems. Working with vendors and partners, you will build hardware and work with our operations staff to deploy it in the field.
With this sensor data and other data sources at KoBold, you will build models and apply a wide range of scientific computing, statistical, and physics-based methods to find places where there is evidence of ore-forming processes at work and to predict the locations of ore-grade mineralization in 2D and 3D. You will help build a worldwide dataset that underlies our exploration program, with careful attention to identifying and quantifying uncertainty in the data and in our predictions. You will be creating models and developing software to accelerate discovery of critical battery metals.
You will join an outstanding team of data scientists and engineers and will work closely with KoBold's world-renowned geoscientists to incorporate our best understanding of the chemical and physical processes that create ore deposits. Working with your geoscience colleagues, you will identify new opportunities and technologies for geophysical data collection, create 2D and 3D geologic predictions, identify exploration targets, design field programs to collect data, and use that data to reduce the uncertainty in our predictions and guide the next phase of field work.
Ultimately, your role is to help KoBold make valuable discoveries by building and deploying next generation hardware and using data tools to solve scientific problems. As one of the early members of this team, you will help build these tools from the ground up.
Responsibilities of this position include:
Technical execution
Design, develop, and deploy new mineral exploration data collection instruments and methods.
Help develop KoBold's proprietary software exploration tools.
Find and curate a wide variety of geospectral, geophysical, geochemical, geologic, and geographic data and integrate it into KoBold's proprietary data system.
Build models to make statistically valid predictions about the locations of compositional anomalies within the Earth's crust.
Create effective visualizations for evaluating model performance and enabling rapid interaction with the underlying data and key features.
Develop and apply a range of data processing, statistical, and physics-based techniques to geoscientific data - from computer vision to geophysical inversions - and use the results to guide our targeting efforts and inform our acquisition and exploration decisions.
Present to and collaborate with our external partners and stakeholders.
Push the state of the art in analysis capabilities by implementing statistically rigorous spatially aware clustering, anomaly detection, and other analysis methods
Collaborate with data scientists, geoscientists and engineers to invent and deploy algorithms that combine large and complex data sets for mineral exploration and discoveries
Qualifications
Demonstrated ability to quickly absorb and synthesize complex information, with a track record of high intellectual rigor in a professional setting.
Exceptional curiosity and eagerness to learn, with a proactive approach to exploring new concepts and technologies.
A successful track record of developing complex equipment with cross-disciplinary teams and vendors.
Technical skills, including extensive experience with:
Physical measurement and data analysis systems that use phenomena such as optics, electromagnetism, radiation, and gravity.
Applying scientific knowledge to identify and prototype emerging technologies
Systems integration and data acquisition.
Python's data science packages and general software engineering practices.
Collaborative software development (git), and familiarity with software engineering best practices like unit test / integration test suites, and CICD pipelines.
SQL, as well as familiarity with non-relational databases.
Cloud computing resources.
Building a wide variety of predictive models, applying them to different problems, and evaluating and interpreting the results.
Data analysis, physics analysis, and applied statistics on a broad range of types of data including data from physical systems.
Capacity to dive deep on novel challenging problems in applying ML to mineral exploration, including understanding a complex domain of geology and mineral exploration practices as well as working with limited, disparate and noisy data sources
Experience deploying sensors in the field
Work practices and motivation:
Ability to take ownership and responsibility of large projects.
Intellectual curiosity and eagerness to learn about all aspects of mineral exploration, particularly in the geology domain. Open to working directly with geologists in the field. Enjoys constantly learning such that you are driving insights and innovations.
Ability to explain technical problems to and collaborate on solutions with domain experts who aren't software developers. A strong communicator who enjoys working with colleagues across the company.
Excitement about joining a fast-growing early-stage company, comfort with a dynamic work environment, and eagerness to take on a range of responsibilities.
Keen not just to build cool technology, but to figure out what technical product to build to best achieve the business objectives of the company.
Ability to independently prioritize multiple tasks effectively.
It is also helpful but not required to have experience with:
Remote sensing
Creating machine learning models on geospatial data
Image processing or computer vision
Project and team management
KoBold Metals is an equal opportunity workplace and an affirmative action employer. We are committed to equal employment opportunity for people of any race, color, ancestry, religion, sex, gender identity, sexual orientation, marital status, national origin, age, citizenship, disability, or veteran status.
This position is Full-time Exempt
Salary is one part of KoBold's total compensation. The US salary range for this role is between $125,000 and $235,000, and will depend on your skills, qualifications, experience, and location. In addition to salary, we offer equity compensation. We also offer benefits including medical, dental, and vision insurance, a 401k retirement plan, short & long term disability and life insurance. We also offer paid sick time and parental leave."
Location: Remote, Candidates can be located anywhere in the United States or Canada. All candidates must be legally authorized to work in the United States or Canada. 10-20% travel required.
Auto-Apply
About the company
At Covera, we're committed to ensuring high-quality healthcare is more than just a promise. That's why we're leading the way in the emerging science of quality, and connecting providers and payers in their shared quest to improve patient outcomes and care quality. By tackling this challenge, we have the ability to impact millions of lives by raising the standard of care nationwide.
Our initial focus is radiology, where an early and accurate diagnosis has a profound impact on the rest of a patient's care journey. Through our work, which uses clinically-validated science-based tools, we're helping doctors enhance their care, ensuring patients get the right diagnosis, and enabling the healthcare system to support quality improvement at scale.
Through our clinical intelligence platform, we have launched programs that help people access the most effective care and provide doctors with AI-powered quality insights and tools to enhance their care. Today, Covera is partnered with leading employers, payers and healthcare organizations across the US, including Walmart and Microsoft. And, with a pipeline representing over 25% of insured Americans, we are in the early stages of improving care quality for all patients across the globe.
About the role
We are looking for a talented AI Scientist with a focus on Deep Learning to join us in our commitment to improve the quality of care for patients in every community across the nation. You will work with an experienced multidisciplinary team of talented AI scientists, data scientists, engineers, and clinicians to leverage unique healthcare data (in the form of MRI/X-Ray/CT images, clinical reports, and beyond). You will have the opportunity to work with extremely diverse and entirely unique radiology and healthcare datasets that extend to all phases of care delivery (referral, diagnosis, therapy, and outcome/follow-up) from the perspective of all key stakeholders (patients, providers, payers). You will utilize state-of-the-art compute resources, both in-house and on cloud.
In this role, you will be expected to:
Create AI algorithms that will be deployed to reduce misdiagnosis in radiology and improve patient care
Investigate, develop and evaluate new AI methods to improve Covera's understanding of radiology reports and images
Drive innovation and publications and represent Covera Health at scientific and industry conferences
Collaborate with data science, clinical and engineering team members to help us build and deploy our clinical research roadmap
Be passionate about improving patient care using AI
Play an active role in further building the Covera team by joining interview panels and contributing to cross-company projects after onboarding
Requirements:
PhD or MS in computer science, math, physics or related discipline.
2+ years of experience after MS or a PhD with a good AI publication record
Strong deep learning background and familiarity with state-of-the-art NLP and/or CV techniques.
Applied programming experience in Python and PyTorch.
Experience conducting independent research.
Excellent ability to work well as an individual contributor as well as within a multidisciplinary team environment
Strong communicator with excellent interpersonal skills and can-do attitude.
Preferred experience:
Exposure to medical imaging applications of AI
Experience training at scale with multi-gpu setups and large volumes of data. Experience with methods such as model and data parallelism, model sharding and mixed-precision training .
Contribution to research communities and/or journals, including NIPS, ICML, ACL, CVPR, MICCAI, etc.
Benefits
Comprehensive medical plans - choose from three plans, including one with 100% of premiums covered for you and your dependents
Vision & Dental
Flexible Time Off - take the time you need, when you need it
Covera Fridays - once a month, Covera takes a fully paid day off to unplug and recharge
401(k) Retirement Plan
Annual Professional Development Stipend to invest in courses, books, or any other professional development related activity
Annual Wellness stipend for fitness, mental health or other wellness expenses
The minimum and maximum base salary for this position ranges from $140,000 - $155,000, in addition to a discretionary bonus and comprehensive benefits package. Final salary will be based on a number of factors including but not limited to, a candidate's qualifications, skills, competencies, experience, expertise and location. Final compensation decisions may occasionally fall outside of the posted range. Salary ranges are periodically reviewed and may be adjusted in response to market trends and company needs.
At Covera Health, we strive to build diverse teams that reflect the people we want to empower through our technology. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. Equal Opportunity is the Law, and Covera Health is proud to be an equal-opportunity workplace and affirmative action employer. If you have a specific need that requires accommodation, please let a member of the People Team know.
Please note: We are unable to sponsor work visas at this time. Applicants must be authorized to work in the United States without sponsorship now or in the future.
Auto-ApplyPharmacovigilance Scientist
Remote job
About Us:
Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit ***************
As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.
Job Title: Pharmacovigilance Scientist
Location: Remote
Role Overview:
The Pharmacovigilance Scientist plays a critical role in the collection, evaluation, and management of drug safety data throughout clinical development. This role supports the monitoring and assessment of adverse events, safety signal detection, and risk management activities to safeguard patient safety and ensure regulatory compliance. The Pharmacovigilance Scientist collaborates with cross-functional teams to maintain the integrity of safety data and contributes to the preparation of safety-related documentation, presentations and aggregate reports. They work closely with the Senior Medical Director, Pharmacovigilance and Safety, to execute pharmacovigilance strategies.
Key Responsibilities:
Safety Data Collection and Review:
Collects, reviews, and analyzes adverse event reports from clinical trials to identify potential safety signals
Supports quality control review of individual case safety reports (ICSRs)
Assists in ongoing safety monitoring activities, including data reconciliation and quality checks to ensure accuracy of safety data.
Supports safety data management activities, including case processing, follow-up, and coding of adverse events
Risk Assessment and Signal Detection:
Assesses clinical safety data to identify, evaluate, and document adverse events and emerging safety concerns.
Contributes to risk-benefit analyses and supports the development of risk mitigation strategies
Pharmacovigilance Documentation:
Supports the preparation and review of pharmacovigilance documents such as Development Safety Update Reports (DSURs), development Risk Management Plans (dRMPs), and relevant sections of clinical trial protocols, IBs and regulatory submissions
Proficient with safety surveillance systems and tools (e.g., Argus, MedDRA, Veeva Vault)
Scientific Expertise:
Maintains current knowledge of relevant therapeutic areas, pharmacology, and drug safety regulations
Conducts literature reviews and safety signal assessments to inform safety evaluations
Cross-Functional Collaboration:
Works closely with clinical operations, regulatory affairs, medical affairs, data management, bioinformatics and project management teams to ensure comprehensive safety oversight
Supports compliance with global pharmacovigilance regulations and company safety policies
Supports the communication and oversight of pharmacovigilance and contract research organization vendors
Supports the project management of safety activities such as aggregate reports, safety team meetings, signal evaluations, etc.
Qualifications:
Advanced degree in life sciences (e.g., PharmD, PhD) or related field
Minimum of 3 years of experience within the pharmaceutical industry, ideally including drug safety experience
Knowledge of good pharmacovigilance practices, drug safety regulations, and clinical trial processes
Understanding of pharmacovigilance regulatory practices including CIOMS, EMA, ICH and FDA guidelines
Experience with adverse event data review, safety signal detection, and safety database management (e.g. Argus, MedDRA, Veeva Vault)
Strong analytical, communication and presentation skills
Strong organizational and project management skills
Ability to collaborate effectively across multidisciplinary teams in a fast-paced environment
Compensation:
An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity.
The anticipated salary range for candidates, Scientist I is $125,000-140,000 and Scientist II is $140,000-155,000 . The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states.
If located within one of our offices in Waltham, MA or Menlo Park, CA, you will be required to go into office 3 days a week.
We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day.
Salary Range for the Role$125,000-$155,000 USD
What We Offer:
A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
Competitive salary and benefits package.
A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
Opportunities for professional growth and development.
Auto-Apply
Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn.
Job Overview
We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Scientist II. This position will be part of the Translational Research and Medicine-Oncology team, with a primary focus on advancing translational research to support oncology programs in clinical trial stages. This individual will be responsible for designing, oversighting, and interpretating translational studies to understand mechanism of action, resistance pathways, and potential new indications. The candidate may also be involved in biomarker analysis to support these translational objectives.
Job Duties and Responsibilities
Develop hypotheses by integrating insights from scientific literature, preclinical and clinical data
Design experiments to support identification of mechanism of action, resistance mechanisms, and potential indications
Manage translational research and biomarker studies conducted with CROs and academic investigators to ensure high-quality, timely delivery of data
Maintain organized, detailed logs of studies and data to ensure accuracy, reproducibility, and compliance with regulatory standards
Present data and insights in internal meetings and cross-functional program team discussions
Key Core Competencies
Scientific curiosity with ability to generate and test hypotheses that inform drug development
Excellent problem-solving and critical-thinking skills to interpret complex data
Strong organizational skills and attention to detail in managing studies, data, and documentation
Strong project management and vendor oversight skills
Adaptability and resilience in a fast-paced, evolving research environment
Education and Experience
PhD degree in a related field of science (Biology, Biochemistry, Molecular & Cellular biology, Cancer Biology, Immunology)
1-3 years of postdoctoral or industry research experience
Familiarity with oncology research preferred
Experience with common biomarker platforms (e.g. NGS, flow cytometry, IHC) preferred
The base salary range for this role is $102,000 to $127,000. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law.
Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.
Confidential Data: All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential.
Compliance: Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Mental/Physical Requirements: Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.
Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) employer
Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Auto-Apply
Absci is a clinical-stage biotechnology company advancing novel therapeutics using generative AI. Our Integrated Drug Creation™ platform combines cutting-edge AI models with a synthetic biology data engine, enabling the rapid design of innovative therapeutics that address challenging therapeutic targets.
Absci is a global company headquartered in Vancouver, WA, and maintains offices in New York City, Switzerland, and Serbia. Learn more at ************* or follow us on LinkedIn (@absci), X (@Abscibio), and YouTube.
About the role
Absci is seeking AI Scientists to join its team of experts advancing generative and predictive modeling at the intersection of machine learning and drug discovery. As an AI Scientist, you will develop AI models that generate and evaluate antibody therapeutic candidates. We are looking for exceptional contributors with backgrounds in deep learning, protein design and engineering, natural language processing, computer vision, and molecular dynamics to develop innovative approaches to creating and assessing therapeutic antibodies
in silico
.
Absci's computational teams (including its AI Scientists) develop and validate software platforms for antibody design and
in silico
assessment, while its Wet Lab teams experimentally validate its AI platforms, and its Drug Creation teams translate experimentally-validated AI designs into clinically-viable therapeutics.
The ideal AI Scientist candidate will:
Care as much about solving the technical problems related to designing antibody therapeutics as they do about translating solutions to the clinic;
Use their expertise to influence the AI team's research agenda while maintaining high levels of responsibility and accountability for their work;
Demonstrate their curiosity about the problems we are attempting to solve by developing proficiency in disciplines that fall outside their own areas of expertise, constantly increasing the scale and impact of their contributions;
Invest in ensuring their work is accessible and interpretable to scientists with other domain expertise.
Why Absci's AI team?
Absci offers AI Scientists a unique opportunity to not only develop novel, cutting edge machine learning models, but also apply these models in real-time to generate candidate antibody therapeutics. In particular:
Absci provides its AI Scientists with access to industry-leading compute resources, enabling large-scale experimentation for model training and deployment.
Absci maintains its own Wet Lab, enabling AI Scientists to validate novel modeling methods via both
in silico
and
in vitro
experimentation.
Absci maintains and is growing its own internal pipeline of assets, enabling AI Scientists to see their work directly translated into therapeutic impact for patients.
This position can be remote, hybrid, or onsite in New York, NY or Vancouver, WA.
Key Responsibilities
Develop state-of-the-art deep learning models for structure-based antibody design, antibody sequence design, antibody-antigen co-folding, antibody-antigen binding prediction, and physics-based antibody design and evaluation
Partner with teammates in AI Research, Platform Engineering, and Computational Biology to identify key challenges and design innovative, AI-driven solutions
Analyze
in silico
and
in vitro
validation results to iteratively improve design and evaluation methodologies
Deliver and publish high-impact research that advances Absci's position as a thought leader in the field of AI antibody design
Qualifications
PhD or equivalent experience in Machine Learning, Computer Science, Computational Biology, Computational Chemistry, Biophysics, or a related field
3+ years of research experience at the intersection of machine learning and protein design, molecular modeling, or a related field, ideally including industry experience
Fluency in Python and PyTorch
Comfortable with design, implementation, and evaluation of state-of-the-art AI algorithms for protein design and protein structure prediction
Expertise in large-scale model training
Demonstrated ability to work collaboratively in an ambitious, fast-paced, interdisciplinary environment
Demonstrated experience presenting complex technical work to diverse audiences
Strong publication record in respected, high-impact journals and conferences
Absci's AI team does not accept and is not responsible for fees related to unsolicited agency resumes.
Compensation and Benefits
The base salary range for this position is $160,000- $260,000. The range provided is based on what we believe is a reasonable estimate for the base salary range for this job at the time of posting. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
Absci offers highly competitive salaries and benefits including medical, dental, and vision insurance, unlimited vacation, parental leave, employee assistance programs, voluntary life and disability insurance, annual bonus potential, the ability to participate in our employee stock purchase plan, a 401(k) with a generous company match, and so much more.
Legal authorization to work in the United States is required. Absci is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, sexual orientation, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, marital status, or any characteristic protected under applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should request the recruiter or hiring manager or contact ****************.
Auto-ApplyOptimization Scientist (1099 Contract)
Remote job
AI
RESILIENCE IN THE FACE OF DISRUPTION. DEFCON AI is an insights company that leverages artificial intelligence, mathematical optimization, data analytics, and software engineering for resilient optimization of complex systems.
In today's dynamically changing world, DEFCON AI's technology aligns outcomes with operational goals, better decision making, and empowers customers to anticipate assess, and mitigate the impacts of disruptions.
About the Optimization Scientist Position
Are you passionate about driving innovation through advanced mathematical modeling? Does working in a multi-disciplinary team that addresses a diverse range of complex problems get you excited? If so, we have an exciting opportunity for you as an Optimization Scientist in the Tech Development and Analytics team at DEFCON AI.
We're currently looking for creative, smart, and humble teammates who want to join our group of world-renowned researchers as we push the boundaries applying AI to complex problems. As an Optimization Scientist, you will be at the forefront of driving the development and deployment of our latest optimization models to production. If you're a forward-thinking, technically adept individual with a passion for mathematical modeling and optimization, this role is for you.
This role is a 1099 contract opportunity, with full time hours.
Responsibilities:
Integrate with an interdisciplinary team of experts in optimization and simulation to design, build, and optimize models that deliver high-quality, real-world insights.
Design and implement novel heuristics and optimization models to solve complex problems in various industries, ensuring efficiency and scalability.
Stay up to date with the latest advancements in decision science and implement best practices for our customers.
The communication of complex technical concepts and findings to non-technical stakeholders clearly and concisely.
Collaborate with cross-functional teams to understand business requirements and translate them into actionable solutions.
Qualifications:
Demonstrated expertise in building mathematical optimization models for complex real-world problems
The ability to write efficient, clean, and maintainable code in one or many programming languages with the ability and willingness to learn more
Excellent written and verbal communication skills - with emphasis on the ability to effectively communicate highly technical concepts to both technical and non-technical audiences alike
An advanced degree in Operations Research, Industrial Engineering, Physics, Mathematics, or a related technical field
U.S. citizenship is required
Preferred Qualifications:
Experience with cloud-based SAAS products and pipelines
Experience with Algebraic Modeling Languages and Solvers (e.g., Pyomo, GAMS, AMPL, CPLEX, Gurobi)
A Ph.D. with a focus on Optimization
Experience in modeling transportation and logistics
Publications in scientific journals and/or conferences
We're an Equal Opportunity Employer: You'll receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability. www.
Auto-ApplyOptimization Scientist (1099 Contract)
Remote job
About Us
Red Cell Partners is an incubation firm building and investing in rapidly scalable technology-led companies that are bringing revolutionary advancements to market in three distinct practice areas: healthcare, cyber, and national security. United by a shared sense of duty and deep belief in the power of innovation, Red Cell is developing powerful tools and solutions to address our Nation's most pressing problems.
About the Optimization Scientist Position
Are you passionate about driving innovation through advanced mathematical modeling? Does working in a multi-disciplinary team that addresses a diverse range of complex problems get you excited? If so, we have an exciting opportunity for you as an Optimization Scientist in the Tech Development and Analytics team at DEFCON AI.
We're currently looking for creative, smart, and humble teammates who want to join our group of world-renowned researchers as we push the boundaries applying AI to complex problems. As an Optimization Scientist, you will be at the forefront of driving the development and deployment of our latest optimization models to production. If you're a forward-thinking, technically adept individual with a passion for mathematical modeling and optimization, this role is for you.
This role is a 1099 contract opportunity, with full time hours.
Responsibilities:
Integrate with an interdisciplinary team of experts in optimization and simulation to design, build, and optimize models that deliver high-quality, real-world insights.
Design and implement novel heuristics and optimization models to solve complex problems in various industries, ensuring efficiency and scalability.
Stay up to date with the latest advancements in decision science and implement best practices for our customers.
The communication of complex technical concepts and findings to non-technical stakeholders clearly and concisely.
Collaborate with cross-functional teams to understand business requirements and translate them into actionable solutions.
Qualifications:
Demonstrated expertise in building mathematical optimization models for complex real-world problems
The ability to write efficient, clean, and maintainable code in one or many programming languages with the ability and willingness to learn more
Excellent written and verbal communication skills - with emphasis on the ability to effectively communicate highly technical concepts to both technical and non-technical audiences alike
An advanced degree in Operations Research, Industrial Engineering, Physics, Mathematics, or a related technical field
U.S. citizenship is required
Preferred Qualifications:
Experience with cloud-based SAAS products and pipelines
Experience with Algebraic Modeling Languages and Solvers (e.g., Pyomo, GAMS, AMPL, CPLEX, Gurobi)
A Ph.D. with a focus on Optimization
Experience in modeling transportation and logistics
Publications in scientific journals and/or conferences
We're an Equal Opportunity Employer: You'll receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.
Auto-ApplyModern AI Scientist
Remote job
Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers' toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: *************************************************************************************** applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Job Description:
AI Scientist - Modern AI Applications
3M Health Care is now Solventum
At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.
We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.
The Impact You'll Make in this Role
As a Principal AI Scientist with deep expertise in Agentic AI, Generative AI, and Natural Language Understanding (NLU), you will lead high-impact technical innovation in HIS applications. In this role, you will be a hands-on research and development leader - driving technical breakthroughs, designing novel AI architectures, and directly influencing the integration of advanced AI into mission-critical healthcare products. You will collaborate closely with other scientists, engineers, and domain experts to create solutions that are explainable, reliable, and transformative for healthcare operations.
Key Responsibilities
Research & Innovation
Design, prototype, and evaluate novel AI models for autonomous, agent-based systems in healthcare workflows.
Advance state-of-the-art NLU for clinical, operational, and administrative healthcare text.
Explore and implement new capabilities in reasoning, decision-making, and multi-modal understanding.
Healthcare-Focused AI Development
Adapt and fine-tune large language models to handle healthcare-specific language, regulatory requirements, and ethical considerations.
Create AI pipelines that can process structured and unstructured healthcare data (FHIR, HL7, clinical notes, claims data).
Contribute to domain-specific model architectures that improve clinical decision-making, revenue cycle management, and patient engagement.
Technical Leadership
Serve as the primary technical authority on Agentic and Generative AI within project teams.
Mentor junior AI scientists and engineers through code reviews, research guidance, and technical workshops.
Drive internal knowledge-sharing on emerging AI trends, frameworks, and best practices.
Operational & Compliance Excellence
Implement rigorous model evaluation frameworks for accuracy, robustness, and fairness.
Ensure compliance with healthcare privacy and data security regulations (HIPAA, HITRUST).
Partner with engineering to move research prototypes into production environments.
Required Qualifications
Master's in Computer Science, AI, Machine Learning, or related field AND 5+ years of experience in AI/ML, with a strong portfolio of deployed models.
Or
PhD in Computer Science, AI, Machine Learning, or related field AND 3+ years of experience in AI/ML, with a strong portfolio of deployed models.
Experience in Python, R, and modern ML libraries.
Experience with GenAI, LLMs, and transformer architectures.
Experience with AI development tools and frameworks (PyTorch, TensorFlow, Hugging Face, LangChain, RAG systems).
Preferred Skills
Multi-modal AI research experience (text, image, structured data).
Knowledge graph integration and symbolic reasoning expertise.
Proven ability to take AI research from concept to production.
Hands-on experience with autonomous AI agents and reasoning systems.
Strong track record applying AI to healthcare or life sciences use cases.
Familiarity with cloud platforms (AWS) and MLOps practices.
Work location:
US Remote
Travel: May include up to 10% domestic
Relocation Assistance: Is not authorized
Must be legally authorized to work in the country of employment without sponsorship for employment visa status (e.g., H1B status).
Supporting Your Well-being
Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.
Onboarding Requirement: To improve the onboarding experience, you will have an opportunity to meet with your manager and other new employees as part of the Solventum new employee orientation. As a result, new employees hired for this position will be required to travel to a designated company location for on-site onboarding during their initial days of employment. Travel arrangements and related expenses will be coordinated and paid for by the company in accordance with its travel policy. Applies to new hires with a start date of October 1st 2025 or later.Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.
Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.
Please note, Solventum does not expect candidates in this position to perform work in the unincorporated areas of Los Angeles County.Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.
Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.
Solventum Global Terms of Use and Privacy Statement
Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.
Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with the
terms.
Auto-ApplyVariant Assessment Scientist I - Oncology (REMOTE, USA)
Remote job
Compensation:
$95,000 - $110,000 per year. You are eligible for a Short-Term Incentive Plan with the target at 5% of your annual earnings; terms and conditions apply.
Variant Assessment Scientist I, Oncology - Remote US
Responsibilities include variant analysis of diagnostic molecular genetic test results; evaluation of published literature, clinical data and review of both functional and in silico data to provide accurate, thorough, and thoughtful clinical interpretation of results. Write research articles in collaboration with other medical professionals and colleagues outside and inside the organization, if data is relevant to the scientific community. Additional responsibilities as designated by supervisor/manager and/or with increasing seniority (Variant Assessment Scientist II, Senior Variant Assessment Scientist).
Essential Functions
Write and interpret molecular test results, including relevant medical literature reviews and summary
Participate in updating variant classification guidelines and developing gene specific classification guidelines
Research novel ways to assess sequence variants
Manage and follow guidelines of variant pre-classification workflow to maximize reporting results within published turn-around times
Assist in the development of gene specific tools and database of gene specific information for variant assessment
Other duties as assigned
Qualifications
PhD and/or MD with expertise in molecular genetics, human genetics, molecular pathology or related field
MS in molecular biology, genetics or a related field with exceptional expertise and outstanding job performance is also considered
Thorough and ongoing knowledge of current theories and principles of human genetics
Excellent written and verbal communication skills to convey difficult information in a clear, kind, and respectful manner
Willingness and ability to work in and contribute to a fast-paced, highly collaborative environment
Preferred:
Prior experience in oncology and variant assessment
#LI-AC1 #LI-REMOTE
PRIVACY NOTICES
To review Ambry's Privacy Notice, Click here: *********************************************
To review the California privacy notice, click here: California Privacy Notice | Ambry Genetics
To review the UKG privacy notice, click here: California Privacy Notice | UKG
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Auto-ApplyClinical Research Scientist Interventional Solutions
Remote job
SummaryAre you looking to make meaningful impact with your research/technical experience? Working daily in close partnership with Interventional key clinical partners - as well as global and local GE Healthcare colleagues - you will be responsible for locally driving the technical and scientific design and execution of collaborative projects, evaluating early developments and generating evidence on new products while providing insights to the global modality on unaddressed clinical needs and growing trends.
GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.Job DescriptionResponsibilities
Support collaboration with top Interventional clinical partners, planning and executing pre- and post-market evidence generation research projects per Interventional research priorities.
Assist in maturing evidence portfolio (writing journal publications/summary articles, technical documents, clinical marketing/training collaterals) and identifying unique opportunities for partnership (contributing to letters of support, research proposals, supporting identified grant submissions).
Support adoption of new technology or clinical applications through advocacy and evidence.
Participate in customer presentations regarding use of Interventional products for institution research purposes.
Closely connected with GEHC global modality clinical and R&D teams, explore unmet clinical and technical needs with external collaborators and translate to define and prioritize product development needs.
Collect data, clinical & product feedback, technical study endpoints, DICOM images and annotations
Support customer satisfaction through communication, observation, and escalation of site inquiries/concerns.
Grow technology leadership mindshare through joint scientific presentations and publications.
Install/upgrade research equipment and software & prototypes
Lead GE Interventional solutions evaluation and optimization for emerging interventional procedures
Represent the global modality technical, scientific and product expertise in USCAN to support local clinical teams and best-in-class customer experience on new products.
Study new technology concepts and leverage expertise to move initiatives forward.
Note:
No sponsorship available for this role now or in the future to work in the United States..
Qualifications
PhD or Master's degree, or foreign degree equivalent, in Medical Imaging, Physics, Computer Science, Biomedical Engineering, or related field.
3+ years of experience in Interventional healthcare industry or research.
Knowledge of Interventional procedures, anatomies, clinical practice.
Excellent written and verbal communication skills.
Excellent customer relationship management and collaboration skills.
Demonstrated clear thinking and problem-solving abilities, a creative mindset, and the ability to quickly grasp new ideas.
Self-starter, able to work independently and collaboratively with partners clinical staff, GE global engineering team and GE regional clinical teams, results oriented, able to multi-task.
Flexible, intellectually curious, and able to work under remote supervision with cross-functional, global teams.
Able to individually lead complex projects with autonomy, rigor, drive & competence
Ability to travel (
Quality, Compliance, and Continuous Improvement focus
Desired Characteristics
5 years' experience in an engineering or science field such as Biomedical Engineering, Medical Imaging, Computer Science, Applied Math or Physics.
Experience in a clinical environment working with clinicians/radiologists/specialists (e.g. interventional radiology or cardiology department)
Demonstrated record of innovation and development.
History of publications, clinical/non-clinical experiments, knowledge in statistics
Programming / Image processing experience
Experience with academic and/or clinical research collaborations
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership -always with unyielding integrity.
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration, and support.
#LI-BR3
#LI-Remote
We will not sponsor individuals for employment visas, now or in the future, for this job opening. For U.S. based positions only, the pay range for this position is $97,600.00-$146,400.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement.Additional Information
GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.
Relocation Assistance Provided: No
Auto-Apply
Zeno Power is the leading developer of nuclear batteries - compact power systems that provide reliable, clean energy in frontier environments. By harnessing the heat from radioisotopes, Zeno's batteries power critical missions on Earth, in space, and at sea. To bring this technology to market by 2027, Zeno is seeking out purpose-driven and innovative professionals who are comfortable working in a startup environment. Team members will have a direct impact in enabling commercial and national security missions from the depths of our oceans, to the surface of the moon, and in austere environments here on Earth. Zeno is proud to be an Equal Opportunity Employer and is committed to attracting, retaining, and developing a highly qualified, diverse, and dedicated work force. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state, or local law.
Scientist
Zeno is seeking a highly motivated Scientist to support the mission-oriented efforts of developing and bringing to market Radioisotope Power Systems (RPS) technologies.
In this role you will:
Support chemistry development of radioisotope power source (RPS) fuel forms from R&D to production stages
Execute fuel development work, including synthesis, purifications, pelletization, and characterization of RPS fuel forms
Perform testing and analysis on existing compounds to capture properties, characteristics, and compatibility with new or existing RPS systems and technologies
Prepare, issue, and present on relevant experimental process, results, and conclusions
Prepare samples for analysis using analytical instrumentation
Plan, perform, and oversee a broad range of experiments from research to quality-controlled process execution
Assist with documenting experimental procedures, hazards assessments, and results
Support Environmental Health & Safety (EH&S) to ensure a safe working environment
Assist with instrument and equipment maintenance and calibration
Support Zeno Power's Nuclear Safety Culture
Key Qualifications and Skills
PhD in Chemistry or B.S. in Chemistry with 4+ years of relevant industry experience
Strong inorganic chemistry experience desired
Hands-on experience in disciplines related to analytical chemistry, inorganic chemistry, and materials science
Ability to follow and develop laboratory safety protocols
Operates with a high degree of trust and integrity, communicates openly, displays respect and a desire to foster teamwork
Experience working in glovebox and/or hot cell environments is desired
Candidate must be a self-starter and possess ability to coordinate and lead laboratory efforts with minimal direction
Can meet deadlines and perform under pressure in an uncertain environment
Must clearly demonstrate the ability to work either independently or as part of a team
Must have excellent written and oral communication skills
Eagerness to learn
Job Functions
Position requires in-office presence in Seattle (South Lake Union) on Tuesdays, Wednesdays, and Thursdays.
Remote work is generally optional on Mondays and Friday in our hybrid environment, but this role may require in-office lab work on these days to support ongoing project needs.
Travel: Travel may be required,
Motor Abilities: Sitting/standing for extended periods, gripping, fine motor control (hands)
Physical requirements: Ability to safely lift up to 15 pounds
Special Senses: Visual and audio
Work Conditions: Typing, standing/sitting working environment of >8 hr/day
Compensation and Benefits
The anticipated salary band for this position is $90,000 - $125,000. The final job level and compensation will be determined by various factors such as a candidate's relevant work experience, years of relevant experience, skills, qualifications, certifications, and other business considerations.
In addition to competitive compensation, we also offer a generous benefits package, which includes:
Stock options
Flexible paid time off
401k plan with employer match
16 weeks of paid family leave
Employer HSA contributions
Transit benefits to put toward commuting expenses
Medical, dental, and vision insurance
Relocation assistance
Dog friendly office
Physical Demands and Work Environment
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions. While performing the duties of this position, the employee is regularly required to talk or hear. Specific vision abilities required by this position include close vision, distance vision, peripheral vision, and the ability to adjust focus. The noise level in the work environment is usually moderate.
Note
This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. All duties and responsibilities are essential functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbents will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. This document does not create an employment contract, implied or otherwise, other than an “at will” relationship.
Export Control
Applicants for employment at Zeno Power must be a U.S. person. The term “U.S. Person” means (i) a U.S citizen or U.S. national; or (ii) any natural person who is a U.S. Lawful Permanent Resident (i.e., holds a Green Card), as defined by 8 U.S.C. 1101(a)(20) or as a “protected individual” defined by 8 U.S.C. 1324b(a)(3) (i.e., admitted as a refugee or is granted asylum).
Fishery Restoration Scientist
Remote job
Seeking a Fishery Restoration Scientist to support NOAA Fisheries in executing analytical, technical, and field-related tasks across multiple habitat conservation and environmental review programs. This position will work closely with the NOAA Project Lead (PL) to evaluate project impacts, conduct habitat analyses, support regulatory reviews, and develop high-quality technical deliverables. The work will be performed in a fully remote capacity, with only a limited possibility of occasional travel within the east coast regions of Florida, South Carolina, North Carolina, or Georgia.
The task includes the following:
* Review study objectives developed by the Southeast Region and project partners, identify optimal field study locations, manage partner-provided datasets, develop associated metadata, and recommend practicable refinements to future field efforts. Deliver short technical reports and data files and incorporate all NOAA PL comments into final documentation.
* Analyze project-specific data to evaluate compliance with hydropower facility license conditions, with particular attention to fish passage and flow prescriptions. Deliver concise written reports for each facility and revise final documentation in response to NOAA PL comments.
* Assess effects to Essential Fish Habitat (EFH) and evaluate proposed mitigative measures for offshore wind energy projects using data provided. Prepare short written reports and develop briefing materials suitable for NOAA senior leadership summarizing project objectives, expected impacts, benefits, and anticipated schedules. Address all NOAA PL comments in final deliverables.
* Review dredging operation data and coral condition information for the Port Everglades and Port Miami project areas. Evaluate potential effects to coral habitat, recommend mitigation measures to offset expected impacts, and deliver a written report containing habitat characterizations and supporting GIS files with appropriate metadata and Google Earth files. Address all NOAA PL comments in final documentation.
* Conduct EFH, Fish and Wildlife Coordination Act (FWCA), and Fish and Wildlife Planning Assistance (FPA) analyses for proposed construction and restoration projects. Maintain a current understanding of diadromous, estuarine, and reef fish habitats, key environmental pressures, and conservation partnerships across Southeast U.S. watersheds. Use GIS to prepare maps and manage spatial data for analysis, and produce written reports and briefing materials with complete responses to NOAA PL comments.
* Submit electronic monthly progress reports that clearly correlate cost, level of effort, activity descriptions, and accomplishments for the reporting period.
Requirements
* Knowledge of fish and habitat ecology, environmental conservation principles, and habitat impact assessment methodologies.
* Experience conducting data analysis, preparing technical summaries, and managing fisheries or environmental datasets.
* Experience using GIS software for spatial analysis, map production, and metadata development.
* Familiarity with EFH assessments, environmental review processes, and habitat-based conservation strategies within marine or estuarine systems.
* Ability to write clear, concise technical reports and prepare briefing materials for senior decision-makers.
* Strong proficiency with common software including word processing, spreadsheets, statistical tools, data management applications, and the entire Google suite.
* Ability to collaborate with partners, manage multiple ongoing tasks, and respond to technical comments with accuracy and completeness.
* Must be a US Citizen or Permanent Resident who has lived in the United States at least 3 of the last 5 years and must be able to pass a background investigation to obtain a security badge to access applicable government systems.
Work Location
This position is fully remote in support of NOAA Fisheries.
Education
Bachelor's degree in Biology, Marine Science, Ecology, Environmental Science, or a related discipline, plus three years of experience in fish biology, marine biology, oceanography, or a closely related field.
Salary
The salary range for this role is $46,000 - 221,000/year. This range is a good faith estimate based on similar roles across the organization. ERT considers several factors when extending an offer of employment, including the location, scope, and associated responsibilities of the specific position, as well as a candidate's work experience, education/training, and key skills.
Benefits
All full-time employees are eligible to participate in our flexible benefits package, which includes:
* Medical, Rx, Dental, and Vision Insurance
* 401(k) retirement plan with company-matching
* 11 Paid Federal Government Holidays
* Paid Time Off (PTO)
* Basic Life & Supplemental Life
* Health Savings Account, Flexible Spending and Dependent Care Flexible Spending Accounts
* Short-Term & Long-Term Disability
* Employee assistance program (EAP)
* Tuition Reimbursement, Personal Development & Learning Opportunities
* Skills Development & Certifications
* Professional Membership Reimbursement
* Employee Referral Program
* Competitive compensation plan
* Discretionary variable incentive bonuses based on factors such as individual performance, business unit performance, and/or the company's performance
* Publication and Conference Presentation Awards with bonuses
ERT is a VEVRAA Federal Contractor and Equal Opportunity employer - All qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.
#LI-Remote
Implementation Scientist
Remote job
Current Employees: If you are currently employed at any of the Universities of Wisconsin, log in to Workday to apply through the internal application process.
The Dissemination & Implementation Launchpad is seeking an Implementation Scientist to join its nationally influential and dedicated team. The successful candidate will contribute to program growth by providing consultations, leading training programs, and collaborating with researchers on a variety of established and newly funded projects. This includes consultations on grant development, study execution, and scale up and dissemination of evidence-based findings. The scientist will take primary responsibility for the qualitative research portfolio and be expected to contribute to training in basic aspects of the methodology but also to innovate and develop competency in more advanced and transdisciplinary uses of qualitative methodology (e.g., rigorous mixed methods and Delphi methodologies). The scientist will extend the use of an implementation approach to research bottlenecks (e.g., recruitment science) to advance translational science.
The Scientist will collaborate with experts across campus and within the community to train research teams and research networks in health innovation development, collaborate on grant applications, and author publications. The Scientist will assist with planning, implementation, and evaluation of novel Dissemination & Implementation Launchpad programs, and prepare scientific presentations and manuscripts to report on evaluation results. The ideal candidate will be self-motivated, highly organized, capable of collaboratively leading and advancing multiple projects, skilled in collaborating with other campus units engaging in Dissemination & Implementation and thrive in a fast-paced environment.
This position may require some work to be performed in-person, onsite, at a designated campus work location. Some work may be performed remotely, at an offsite, non-campus work location.
This position has been identified as a position of trust with access to vulnerable populations. The selected candidate will be required to pass an initial caregiver check to be eligible for employment under the Wisconsin Caregiver Law and every four years.
Key Job Responsibilities:
Identifies research problems and develops complex research methodologies and procedures
Serves as a unit subject matter expert and liaison to internal and external stakeholders providing advanced level information and representing the interests of a specialized research area
Collects and analyzes complex research data, conducts experiments and interviews, and documents results according to established policies and procedures under general supervision
Conducts literature reviews, prepares reports and materials, and disseminates information to appropriate entities
Attends and assists with the facilitation of scholarly events and presentations in support of continued professional development and the dissemination of research information
Takes leadership role in developing D&I launchpad's qualitative research consult program, education, tools and other resources in alignment with Launchpad/ICTR grant commitments
Writes or assists in developing grant applications and proposals to secure research funding
May supervise the day-to-day activities of a research unit as needed
Contributes to D&I Launchpad programs and research, including development of implementation and dissemination materials
Monitors program budget and approves unit expenditures
Department:
School of Medicine and Public Health, Institute for Clinical and Translational Research (ICTR), Dissemination and Implementation Launchpad
The Dissemination and Implementation Launchpad Team is part of the UW Institute for Clinical and Translational Research (ICTR) within the School of Medicine and Public Health. We support junior and senior researchers with tools, resources, and scientific guidance to help them move their research findings from experimental settings into clinical and community practice ('translating' research into practice). As a nationally recognized program in dissemination and implementation science, the Dissemination and Implementation Launchpad is at the leading edge of a growing and innovative field, assisting research teams to bridge the gap between research and practice. The Dissemination and Implementation Launchpad team includes faculty, scientists, educators, business consultants, and evaluation professionals and collaborates closely with ICTR's rapidly growing Learning Health System (LHS) program.
Compensation:
The expected salary range for this position is $70,000 up to $104,000 for highly experienced candidates and actual pay within this range will depend on experience and qualifications.
Employees in this position can expect to receive benefits such as generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits. For more information, refer to the campus benefits webpage. SMPH Academic Staff Benefits Flyer
Required Qualifications:
Expertise and professional experience in qualitative research and methods
A minimum of two years of experience with implementation science
Preferred Qualifications:
Experience using and facilitating a variety of qualitative approaches to inquiry in health care such as Delphi process and appreciative inquiry
Education:
Ph.D. in Implementation Science, Public Health, or related field is required
How to Apply:
To apply for this position, select either “I am a current employee” or “I am not a current employee” under Apply Now. You will then be prompted to upload your application materials.
Important: There is only one attachment field. All required documents must be combined into a single file and uploaded in that field.
Required documents:
• Cover letter
• Resume
Your cover letter should address how your training and experience align with the required and preferred qualifications listed above. Application reviewers will rely on these written materials to determine which applicants move forward in the process. References will be requested from final candidates. All applicants will be notified once the search concludes and a candidate is selected.
University sponsorship is not available for this position, including transfers of sponsorship and TN visas. The selected applicant will be responsible for ensuring their continuous eligibility to work in the United States (i.e. a citizen or national of the United States, a lawful permanent resident, a foreign national authorized to work in the United States without the need of an employer sponsorship) on or before the effective date of appointment. This position is an ongoing position that will require continuous work eligibility. If you are selected for this position you must provide proof of work authorization and eligibility to work.
Contact Information:
Kim McFarlane, ********************
Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information.
Institutional Statement on Diversity:
Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals.
The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world.
The University of Wisconsin-Madison is an Equal Opportunity Employer.
Qualified applicants will receive consideration for employment without regard to, including but not limited to, race, color, religion, sex, sexual orientation, national origin, age, pregnancy, disability, or status as a protected veteran and other bases as defined by federal regulations and UW System policies. We promote excellence by acknowledging skills and expertise from all backgrounds and encourage all qualified individuals to apply. For more information regarding applicant and employee rights and to view federal and state required postings, visit the Human Resources Workplace Poster website.
To request a disability or pregnancy-related accommodation for any step in the hiring process (e.g., application, interview, pre-employment testing, etc.), please contact the Divisional Disability Representative (DDR) in the division you are applying to. Please make your request as soon as possible to help the university respond most effectively to you.
Employment may require a criminal background check. It may also require your references to answer questions regarding misconduct, including sexual violence and sexual harassment.
The University of Wisconsin System will not reveal the identities of applicants who request confidentiality in writing, except that the identity of the successful candidate will be released. See Wis. Stat. sec. 19.36(7).
The Annual Security and Fire Safety Report contains current campus safety and disciplinary policies, crime statistics for the previous 3 calendar years, and on-campus student housing fire safety policies and fire statistics for the previous 3 calendar years. UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department.
Auto-ApplyUiPath Robotic Process Automation Developer Associate
Remote job
Type of Requisition:
Regular
Clearance Level Must Currently Possess:
None
Clearance Level Must Be Able to Obtain:
Secret
Public Trust/Other Required:
None
Job Family:
Data Science and Data Engineering
Job Qualifications:
Skills:
Collaborating, Design, Technical Requirements
Certifications:
None
Experience:
0 + years of related experience
US Citizenship Required:
Yes
Job Description:
Own your opportunity to turn data into measurable outcomes for our customers' most complex challenges. As an UiPath Robotic Process Automation Developer Associate at GDIT, you'll power innovation to drive mission impact and grow your expertise to power your career forward.
The UiPath Robotic Process Automation Developer Associate will find themselves at the heart of GDIT's customer-centric approach, playing a pivotal role in ensuring our customers successfully meet their strategic goals. They will use their UiPath expertise and their project skills to develop and promote organizational goals to completion. If you enjoy collaborating with others in a fast-paced environment, you will find this role to be both rewarding and challenging.
MEANINGFUL WORK AND PERSONAL IMPACT
As an UiPath Robotic Process Automation Developer Associate, the work you'll do at GDIT will be impactful to the mission of our customers. You will play a crucial role in the following areas:
Design, develop, test, and deploy solutions built in UiPath; may also utilize Microsoft Power Platform (Power Apps and Power Automate)
Develop flows and automation with UiPath to increase efficiency and effectiveness of organization.
Develop easy-to-use interfaces and forms in UiPath forms/apps to drive business processes.
Collaborate with end users, stakeholders, and management to identify business process needs, document the business and technical requirements, and determine the best automation solutions.
Create process, technical architecture, design, and user guide documentation.
Support architecture and design of UiPath roadmaps.
Participate in development and test teams driving the design, creation, testing, and delivery of technical functionality.
Collaborate with GDIT and customer personnel to establish and maintain automation infrastructure.
Implement best practices in code review, troubleshooting, debugging, and post-implementation support.
Contribute to the development of IT related, technical processes reviews, postmortems, and continual process improvement internally as well as for customers/stakeholders.
Collaborate with technical staff to define implementation and process best practices.
Scope work and create estimations of effort.
WHAT YOU'LL NEED TO SUCCEED
Bring your expertise and drive for innovation to GDIT. The UiPath Robotic Process Automation Developer Associate must have:
● Education: Technical Training, Certifications or Degree
● Experience: 0+ years of related experience
● Required Skills:
Proficiency with UiPath design, development, testing, and deployment
Understanding of UiPath automation frameworks
Ability to identify and solve complex problems
Capability to learn new technologies quickly.
Excellent collaboration skills and can effectively work in a team environment.
Ability to effectively manage multiple competing priorities at any given time.
Ability to work independently and as part of a team
Excellent communication and presentation skills with the ability to present complex insights to both technical and non-technical audiences.
Strong analytical skills with the ability to collect, organize, analyze, and disseminate insights with attention to detail and accuracy.
● Preferred Skills:
UiPath Automation Developer Associate and/or Automation Developer Professional Certification(s)
Proficiency with Microsoft Power Platform (Power Apps and Power Automate) design, development, testing, and deployment
Excel background; familiarity with other Microsoft tools (Outlook, Word, Excel, PowerPoint)
Exposure to ServiceNow.
Knowledge of ITIL framework.
Knowledge of Agile methodology.
Experience with additional coding languages such as Python, R, JAVA, C#. VB.Net, SQL
Previous experience in the defense or government sector a plus
● Security Clearance Level: Must be able to obtain a Secret clearance
● US Citizenship Required
● Location: Ability to commit to a hybrid work model at GDIT's Integrated Technology Center in Bossier City, LA is strongly preferred
GDIT IS YOUR PLACE
At GDIT, the mission is our purpose, and our people are at the center of everything we do.
● Growth: AI-powered career tool that identifies career steps and learning opportunities
● Support: An internal mobility team focused on helping you achieve your career goals
● Rewards: Comprehensive benefits and wellness packages, 401K with company match, and competitive pay and paid time off
● Flexibility: Full-flex work week to own your priorities at work and at home
● Community: Award-winning culture of innovation and a military-friendly workplace
OWN YOUR OPPORTUNITY
Explore a career in data science and engineering at GDIT and you'll find endless opportunities to grow alongside colleagues who share your determination for solving complex data challenges.
The likely salary range for this position is $55,250 - $74,750. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this range.
Scheduled Weekly Hours:
40
Travel Required:
Less than 10%
Telecommuting Options:
Hybrid
Work Location:
Any Location / Remote
Additional Work Locations:
Total Rewards at GDIT:
Our benefits package for all US-based employees includes a variety of medical plan options, some with Health Savings Accounts, dental plan options, a vision plan, and a 401(k) plan offering the ability to contribute both pre and post-tax dollars up to the IRS annual limits and receive a company match. To encourage work/life balance, GDIT offers employees full flex work weeks where possible and a variety of paid time off plans, including vacation, sick and personal time, holidays, paid parental, military, bereavement and jury duty leave. GDIT typically provides new employees with 15 days of paid leave per calendar year to be used for vacations, personal business, and illness and an additional 10 paid holidays per year. Paid leave and paid holidays are prorated based on the employee's date of hire. The GDIT Paid Family Leave program provides a total of up to 160 hours of paid leave in a rolling 12 month period for eligible employees. To ensure our employees are able to protect their income, other offerings such as short and long-term disability benefits, life, accidental death and dismemberment, personal accident, critical illness and business travel and accident insurance are provided or available. We regularly review our Total Rewards package to ensure our offerings are competitive and reflect what our employees have told us they value most.We are GDIT. A global technology and professional services company that delivers consulting, technology and mission services to every major agency across the U.S. government, defense and intelligence community. Our 30,000 experts extract the power of technology to create immediate value and deliver solutions at the edge of innovation. We operate across 50 countries worldwide, offering leading capabilities in digital modernization, AI/ML, Cloud, Cyber and application development. Together with our clients, we strive to create a safer, smarter world by harnessing the power of deep expertise and advanced technology.Join our Talent Community to stay up to date on our career opportunities and events at
gdit.com/tc.
Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans
Auto-ApplyAssociate Scientist (JP9834)
Remote job
Employment Type: Contract Business Unit: Pre-Pivotal DP Synthetic Enabling Technology Duration: 1+ year Rate: $20-22/Hr 3 Key Consulting is hiring an Associate Scientist for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Title: Project Manager - REMOTE - (JP9268)
Location: Thousand Oaks, CA. (100% REMOTE)
Employment Type: Contract
Business Unit: Medical Device Supply and Raw Materials
Duration: 1+ years (with likely extensions)
Notes:
Posting Date: 10/14/2021
3 Key Consulting is hiring a Project Manager for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
In this laboratory-based on-site position, you will work within a cutting-edge solid-state chemistry team to support drug development. You will perform several functions and work across Process Development sites as you use solid state characterization tools to derive knowledge that will help drive efficient development and scalable understanding of processes and products in client's small molecule pipeline.
The ideal candidate would possess:
Proficiency in solid state characterization techniques, such powder X-ray diffraction, particle analysis by laser diffraction, thermal analysis (TGA/DSC), optical microscopy, surface area measurement.
Attention to detail, adaptability to new techniques and multiple tasks, ability to solve problem and meet deadlines, and effectiveness to work independently and as a team member.
Strong computer skills in instrumentation and data processing in a client-server environment.
Excellent communication (verbal and written) and organizational skills.
Why is the Position Open?
Planned project.
Top Must-Have Skill Sets:
Experience with solid state characterization techniques. 1-2 years experience
Strong knowledge in physical and organic chemistry. Bachelors degree in chemistry or chemical engineering
Good verbal and written communication skills
Day to Day Responsibilities:
Perform solid state characterization measurements and analyses.
Design and conduct experiments for form screening and form characterization analysis by following instructions and guidance from project representatives.
Interpret data, maintain timely documentation (i.e. electronic notebooks), and contribute to technical reports and presentations in a cross-functional team environment.
Participate in lab housekeeping, maintain lab equipment and supplies, and comply with lab safety guidelines.
May work occasionally on flexible schedule, i.e. starting early morning or finishing late evening, depending on the project need
Basic Qualifications:
B.S. with degree in Chemistry, Chemical Engineering, Materials Science, Pharmaceutical Science or related scientific background experience. Pharmaceutical/biotech industry experience preferred, but not required.
Demonstrated knowledge of various solid-state characterization techniques such as XRPD, TGA, DSC, particle size, microscopy, surface area, DVS, etc.
Good written and oral communication skills.
Employee Value Proposition:
Candidate would be interfacing with many function areas. Candidate would have a great connection to the pharm development. This is a great hands-on experience and position.
Red Flags:
No background in physical science
No hands on experience with web chemistry labs
Interview process:
Phone screening followed by in-person interview.
We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
hts reserved.
Regards, 3KC Talent Acquisition Team
Easy ApplyGenerative AI Scientist
Remote job
Egen is a fast-growing and entrepreneurial company with a data-first mindset. We bring together the best engineering talent working with the most advanced technology platforms, including Google Cloud and Salesforce, to help clients drive action and impact through data and insights. We are committed to being a place where the best people choose to work so they can apply their engineering and technology expertise to envision what is next for how data and platforms can change the world for the better. We are dedicated to learning, thrive on solving tough problems, and continually innovate to achieve fast, effective results. If this describes you, we want you on our team.
Want to learn more about life at Egen? Check out these resources in addition to the job description.
Meet EgenLife at EgenCulture and Values at EgenCareer Development at EgenBenefits at Egen
About the opportunity: In this role, you'll join our growing team focused on building Generative AI applications for document summarization, classification, and question and answer using unstructured and structured data. This team works with companies of all sizes, from startups to Fortune 100, that are leaders in their fields, pushing the limits of possible. You will develop applications on Google Cloud, work with customers to understand their requirements, suggest new ideas and features to the team, improve the product further, and implement the new functionalities with a passion for quality. You will implement best practices and state-of-the-art techniques for AI and LLMs and work on research, experimentation, and implementation of novel methods.Qualifications:
Required hands-on experience designing and implementing applications using Large Language Models (LLM). More specifically:
Python programming.
Google Gemini, OpenAI GPT, LLaMA, or similar models.
LangChain, LlamaIndex, or similar frameworks.
Advanced prompt engineering.
Retrieval Augmented Generation (RAG).
Vector databases (GCP Vector Search, ChromaDB, Pinecone, pgvector, or similar).
The ideal candidate will also have experience in one or more of the following:Bachelor's or Master's degree in Computer Science, Engineering, or related field.
LLM model fine-tuning.
Embedding model fine tuning.
Shell scripting.
Google Cloud Vertex AI (AutoML, AI APIs, etc.).
Classic Machine Learning (ML frameworks, neural net models development, training, tuning, serving).
MLOps (ideally on GCP).
Data Engineering (including SQL).
Personal Attributes:
Strong ethics.
Strong technical aptitude.
Engineering mindset/developer background.
Strong sense of ownership and teamwork.
Curious, always learning to get better.
Enjoys working with clients.
Excellent communication skills.
Compensation & Benefits:
This role is eligible for our competitive salary and comprehensive benefits package to support your well-being:- Comprehensive Health Insurance- Paid Leave (Vacation/PTO)- Paid Holidays- Sick Leave- Parental Leave - Bereavement Leave- 401 (k) Employer Match- Employee Referral Bonuses
Check out our complete list of benefits here - >********************************
Important: All roles are subject to standard hiring verification practices, which may include background checks, employment verification, and other relevant checks.
EEO and Accommodations:
Egen is an equal opportunity employer and is committed to inclusion, diversity, and equity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veterans' status, or any other characteristic protected by federal, state, or local laws. Egen will also consider qualified applications with criminal histories, consistent with legal requirements. Egen welcomes and encourages applications from individuals with disabilities. Reasonable accommodations are available for candidates during all aspects of the selection process. Please advise the talent acquisition team if you require accommodations during the interview process.
Auto-ApplySenior Toxicologist
Remote job
Are you looking to join an organization that is growing and dynamic? What about a high-energy, collaborative environment that rewards hard work? J.S. Held is a global consulting firm that combines technical, scientific, financial, and strategic expertise to advise clients seeking to realize value and mitigate risk. Our professionals serve as trusted advisors to organizations facing high stakes matters demanding urgent attention, staunch integrity, proven experience, clear-cut analysis, and an understanding of both tangible and intangible assets. The firm provides a comprehensive suite of services, products, and data that enable clients to navigate complex, contentious, and often catastrophic situations.
Provide expert toxicological analysis and consulting on matters involving human health risk, chemical exposure, product safety, and regulatory compliance.
Review and interpret toxicological data, exposure assessments, and risk evaluations.
Serve as a subject matter expert in litigation support and regulatory.
Maintain strong relationships with existing and prospective clients.
Develop proposals, scopes of work, and pricing strategies for toxicology-related services.
Not expected to serve as a testifying expert.
Qualifications
Ph.D. in Toxicology or board certification if the Ph.D. is in a related field.
Minimum of 5 years of professional experience managing complex toxicology projects.
A consulting background is desirable but not mandatory.
Strong understanding of regulatory frameworks (e.g., REACH, CLP, OSHA, EPA, etc.).
Proven success in client relationship management.
Excellent communication, presentation, and interpersonal skills.
Strong technical writing skills.
High attention to detail and enjoys working on a variety of different projects simultaneously.
Additional Information
Some of the Benefits We Have Include
J.S. Held understands all our employees are people and sometimes life needs flexibility. We work to always provide an environment that best supports and suits our team's needs.
Our flexible work environment allows employees to work remotely, when needed
Flexible Time Off Policy
Medical, Dental, and Vision Insurance
401k Match
Commuter Benefits
A reasonable estimate of the salary range for this role is $150,000 - $180,000. Any offered salary range is based on a wide array of factors including but not limited to skillset, experience, training, location, scope of role, management responsibility, etc.
Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
By submitting your application, you acknowledge that you have read the J.S. Held Online Privacy Notice and hereby freely and unambiguously give informed consent to the collection, processing, use, and storage of your personal information as required and described therein. California residents can click here to learn more about the personal information we collect and here to learn about additional privacy rights that may be available.
Please explore what we're all about at ***************
EEO and Job Accommodations
We embrace diversity and our commitment to building a team and environment that fosters professional and personal enrichment is unwavering. We are greater when we are equal! J.S. Held is an equal opportunity employer that is committed to hiring a diverse workforce. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin,
disability, protected Veteran status, age, or any other characteristic protected by law. If you are an individual with a disability and would like to request for a reasonable accommodation, please email
[email protected]
and include “Applicant Accommodation” within the subject line with your request and contact information.
#LI-IM1
Zoetis Veterinary Medicine Research and Development (VMRD) seeks a skilled Toxicologist to join the Toxicology Group within Clinical Pharmacology and Safety Sciences based in Kalamazoo, MI. This challenging and dynamic role provides global toxicology and safety assessment support. The successful candidate will collaborate across VMRD and Global Manufacturing and Supply (GMS) to develop scientifically rigorous safety assessments supporting product safety across therapeutic areas, veterinary species, human health, and manufacturing processes.
Responsibilities:
Toxicological Assessment for Drug Products: Conduct safety assessments for formulation excipients, degradants, raw materials, and residual solvents in active pharmaceutical ingredients (APIs) and drug products
Toxicological Assessment for Manufacturing: Qualify impurities in the manufacturing process of APIs and drug products; conduct safety assessments for extractables and leachables, cross-contamination of products in shared facilities, and establish cleaning limits.
Occupational Safety: Develop Occupational Exposure Limits (OELs/ OEBs) following Zoetis processes and procedures.
User and Worker Safety: Provide product user and worker safety support for project teams, including risk assessments, exposure scenario calculations, risk mitigation proposals, packaging recommendations and label language development.
Safe Exposure Level Development: Establish Threshold of Toxicological Concern (TTC) and health-based exposure limits, including Permitted Daily Exposure (PDE), Acceptable Daily Intake (ADI), and Margin of Exposure (MoE).
Health Hazard/ Medical Assessments: Support pharmacovigilance, product quality, and qualification of out-of-specification batches.
Regulatory Support: Assist with REACH registration for API intermediates and raw materials, and address global regulatory queries related to the safety of registered products.
Toxicology Data Analysis & Literature Review: Perform rigorous toxicology gap analysis, literature data mining, and critical evaluation of toxicological information to support product development and registration.
Hazard Communication and Chemical Regulatory Compliance (Preferred): Experience in preparing Safety Data Sheets (SDS), classifying drug substances and process intermediates according to the Globally Harmonized System (GHS) and national requirements, and horizon scanning and monitoring of chemical regulations.
Cross-Collaboration and Technical Leadership: Engage in multidisciplinary collaboration within R&D, and with Manufacturing, Product Quality, and Sustainability, to develop and integrate key knowledge areas and expertise into actionable business insights.
Regulatory & Scientific Engagement: Support regulatory compliance, trade association participation, and involvement in professional organizations relevant to toxicology.
Travel Requirement: This role involves up to 10% travel for collaborations, regulatory engagements, or conferences as needed.
Minimum Qualifications
Ph.D. (or equivalent) plus at least 2-3 years of experience in toxicology or closely related discipline is critical. Master's degree in toxicology or closely related discipline with 8 years of relevant experience shall be considered.
Demonstrated experience in preparing regulatory-quality technical documents or toxicology dossiers, with strong technical writing skills (e.g., protocols, reports, journal articles)
Experience in study design, implementation, and interpretation of studies evaluating in vivo and in vitro toxicity or similar experience.
Highly organized with strong problem-solving skills, capable of performing rigorous scientific assessments.
Ability to prioritize tasks, make informed decisions, and collaborate effectively in a global matrix environment.
Excellent verbal and written communication skills in English.
Proficiency in MS Office, and toxicology databases for literature research and data analysis
Desirable Skills, Experience, and Attributes:
Board certification in toxicology (e.g., DABT, ERT) and/or DVM.
Knowledge of global regulatory requirements for toxicology risk assessment and documentation to support product safety and chemical registrations.
Experience in preparing safety data sheets.
The following base pay range reflects the anticipated base pay for this position if a selected candidate were to be located in (Colorado). Base pay may vary based on location and other factors.
Base Pay Range: $91,000 - $131,000
The following base pay range reflects the anticipated base pay for this position if a selected candidate were to be
located in (California), (NJ Remote), (NY Remote), or (Washington). Base pay may vary based on location and other factors.
Base Pay Range: $103,000 - $148,000
[This position is eligible for short-term incentive compensation.] [The position is also eligible for long-term
incentive.]
We offer a competitive and comprehensive benefits package, which includes healthcare, dental coverage, and retirement savings benefits along with paid holidays, vacation and disability insurance.
Full time RegularColleague
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.
Auto-Apply