Senior Principal Scientist Jobs in Mississippi

Primary Purpose: In partnership with the Chief Executive Officer (CEO) and the executive leadership, this position is responsible for the coordination of communication, resources, and information to meet school and district needs within curricular areas. Skills and Qualifications: Skilled in identifying problems and brainstorming potential solutions Possesses excellent written and oral communication skills Comfortable working independently and collaboratively with other team members Able to meet aggressive deadlines Education/Certification: Bachelors degree in education, psychology, or related field 5+ years proven experience in an educational consulting role Strong communication and presentation skills Highly professional, organized and detail-oriented Ability to manage multiple projects simultaneously with a constant eye on quality Major Responsibilities and Duties Working knowledge of instructional methods, techniques, principles and theories of education Provide quality coaching, mentoring, and professional development to identified school-level personnel Working knowledge of classroom techniques and academic activities at each educational level. Design new training programs and offer teacher training workshops Ability to plan and teach workshops related to the educational program/project. Use multiple sources of data to establish educational goals and deliver professional development and technical assistance resulting in increased achievement of students Use student work and performance data to evaluate the effectiveness of provided services Research and maintain current knowledge of new and emerging educational techniques in the desired content area Work independently with little direction Working conditions Mental demands/Physical demands/Environmental factors Maintain emotional control under Travel is Occasional prolonged and irregular Stand, walk, crouch, and do moderate lifting up to 40 Reports to: Director of Operations Salary/Retainer: Commensurate with experience Department: Operations

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Biology who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented accounting and tax experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by… Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to Biology Evaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise: A bachelor's or higher degree in Biology or a related subject Experience working as an Biology professional Ability to write clearly about concepts related to Biology in fluent English Payment: Currently, pay rates for core project work by Biology experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project. PLEASE NOTE: We collect, retain and use personal data for our professional business purposes, including notifying you of opportunities that may be of interest and sharing with our affiliates. We limit the personal data we collect to that which we believe is appropriate and necessary to manage applicants' needs, provide our services, and comply with applicable laws. Any information we collect in connection with your application will be treated in accordance with the Outlier Privacy Policy and our internal policies and programs designed to protect personal data. This is a 1099 contract opportunity on the Outlier.ai platform. Because this is a freelance opportunity, we do not offer internships, sponsorship, or employment. You must be authorized to work in your country of residence. If you are an international student, you may be able to sign up for Outlier if you are on a visa. You should contact your tax and/or immigration advisor with specific questions regarding your circumstances.

Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world. At Pfizer, we are always seeking to deliver breakthroughs that change patients' lives. In this role, you'll be working to help us achieve that goal by advancing biotechnologically derived products to the market through innovation and delivery of cutting-edge analytical testing. You will be part of a team which is focused on developing methods and strategies to support product and process development for biotherapeutics and vaccines, including antibodies, antibody-drug conjugates and therapeutic proteins, at all stages of clinical development. You will work across analytical functions and projects and will also play a role in developing leaders and providing technical counsel to other organizations and senior leadership. As a Senior Principal Scientist, you will be at the center of our operations and you'll find that everything we do, every day, is in line with an unwavering commitment to quality. You will be recognized as an outstanding scientist in your group. With your advanced knowledge of the discipline, you will regularly contribute in multi-disciplinary teams representing the department and influencing cross-functional teams. Your innovation is seen in way you promote the use of novel experimental approaches, create processes, hypotheses and methodologies. You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience. You will be entrusted with setting objectives and planning resource requirements for projects. You will undertake mentoring activities to guide team members. It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe. **Responsibilities** * Apply technical and functional knowledge to design and independently execute experiments/projects, contributing to the overall direction of project. Technical areas anticipated: HPLC, LC-MS, dissolution, and spectroscopy (IR,NIR, Raman). * Act as a scientific resource within own sub-function/therapeutic area/discipline. * Develop appropriate drug product analytical control strategies that are aligned with program and regulatory expectations. * Provide technical and scientific leadership and represent analytical development on cross functional and cross-departmental program level teams. * Develop assay, qualification and transfer timelines which align with the program timelines. * Manage individual lab work on drug product candidates with a focus on developing the analytical methods and strategies to support the clinical and commercial aspects of product and process development and controls. * Encourage interaction and effective collaboration with project team members, including presenting data at project team meetings; critical review of data; and active involvement in solving technical challenges that arise during development. * Ensure that the staff has received appropriate training and that the training is current. * Keep abreast of scientific/ technological developments by participating in scientific meetings/ seminars and through regular scientific review. * Present experimental results at group meetings, project meetings and department meetings. * Responsible forthe analytical strategies for development of drug product candidates, which may include method development, release and stability testing, characterization and comparability analyses and analytical support for process and formulation development. * Serve as an analytical sciences resource for the department and project teams, proactively keeping colleagues updated with current scientific trends and technical aspects from conferences, local meetings and literature. **Required Qualifications** * Doctoral Degree (PhD) in Analytical Science. * 7+ years of experience in drug product pharmaceutical development function. * Excellent written communication skills, including the ability to maintain an accurate. scientific notebook and draft concise written reports, publications and related documents. * Experienced with multiple software platforms and packaged, facilitating large data analytics and visualization. * Strong technical skills and scientific expertise in analytical method development and troubleshooting. * Additional analytical skills: NMR, particle characterization, forensic analysis preferred. Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. **NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS** * Travel anticipated to be less than 10% **Additional Information** * Relocation support available. * Work Location Assignment: On Premise The annual base salary for this position ranges from $117,300.00 to $195,500.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.Relocation assistance may be available based on business needs and/or eligibility. **Sunshine Act** Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. **EEO & Employment Eligibility** Pfizer 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. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as we

Key Responsibilities: * Apply and methodology, including the concepts of Statistical Process Control (SPC), to process and experimental data to identify trends, assess process capability, and provide appropriate conclusions to enable data driven decision-making and to determine the root cause of process upsets. * Support of the real-time multivariate SPC programme using SIMCA-online. * Collaborate with laboratory and process scientists on the development of Raman spectroscopy based chemometric models * Use appropriate statistical methodologies to assign specifications, validation acceptance criteria, tech transfer criteria, material sampling criteria, comparability assessments and analysis of batch data for summary reports and product reviews. * Use of statistical and programming software (e.g. SAS, R, JMP, Python, SIMCA) to apply a broad range of data science and statistical applications, such as linear regression, DoE, multivariate analysis, and statistical modelling. * Assist with Design of Experiments (DoE) including data analysis to support lab studies and assist with the development of product control strategies * Interpret and communicate the results of data analytics and statistical analysis clearly and concisely to audiences with varying backgrounds and degrees of technical understanding. * Provide training and mentoring to technical staff to strengthen capabilities in statistical methods and data-based decision making. * Collaborate within cross-functional teams to integrate data analytics and statistical methodologies into everyday work, develop solutions, gain alignment, and deliver impactful business insights while engaging the necessary stakeholders to enable data driven decision-making. * Ensure data integrity by performing rigorous error checking, and data validation. Pre-Requisites * A demonstrated interest in the field of statistics and data science * Skilled in quantitative analysis and data management * Strong problem solving skills * Demonstrated learning agility * Strong ability to influence * Ability to communicate effectively with all levels and functions in the organisation. * Ability to work on multiple concurrent project initiatives. * Ability to work in a team environment * Ability to build strong relationships across the organisation * Highly motivated Educational/Experience Requirements * Third level qualification (eg. BSc or MSc) in Statistics, Data Science, Applied Mathematics or a relevant discipline. * Prior experience in a pharmaceutical manufacturing environment is preferable. * Prior knowledge and experience with programming, data analysis and process modelling in tools such as Python, R, Matlab, Unscrambler, SAS, SIMCA, Grams, JMP, etc. is preferable. Additional Skills/Preferences: * Familiarity in areas like biochemistry, cellular biology, organic chemistry, physical chemistry, and cellular proliferation methods and techniques is desired. * Knowledge of pharmaceutical process steps such as biologics manufacturing, small molecule organic synthesis, and oral solid dosage form manufacturing is advantageous. Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly\_Recruiting\_************************** ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response. Location Indianapolis, Indiana, USA

> Senior Scientist / Principal Scientist, Biotransformation Senior Scientist / Principal Scientist, Biotransformation • DMPK Description *Note: exact level depending on experience* Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide footprinting of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”. Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space. We are uniquely structured with opportunities for all scientists to contribute to both established programs as well as ongoing early target selection, screens and validation. We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression. Vividion was ranked #2 mid-size company on The San Diego Union-Tribune's 2022 and 2023 Top Workplaces list. Job Summary: We are seeking a very highly motivated, collaborative biotransformation expert who is passionate and dedicated to using DMPK expertise to drive drug discovery and development programs at Vividion. The DMPK biotransformation scientist will be responsible for metabolite profiling and identification, as well as enzymology. This is a technical position and the role involves providing scientific and strategic input, guiding medicinal chemists in chemical series optimization, problem-solving and cross-functional collaboration, and innovation in a team environment. The successful candidate will design, execute, and manage in vitro soft-spot and tox species selection MetID studies, and definitive in vivo MetID studies. This role involves both experimental laboratory-based work and management of biotransformation studies conducted at CRO's. The successful candidate is expected to be well-versed in the interpretation of mass spectra, and proficient in the preparation of data summaries, presentation of results to project teams and management, authoring regulatory reports, and contributing to regulatory documents to support clinical development. Requirements Essential Duties and Responsibilities: * Design and conduct unlabeled and radiolabeled in vitro and in vivo biotransformation studies supporting drug discovery and development * Execute in vitro soft-spot and tox species selection MetID studies and conduct in vivo MetID studies. * Manage and provide oversight for biotransformation studies conducted at CRO's * Interact with multidisciplinary project teams * Lead DMPK studies supporting preclinical and clinical development * Work collaboratively across functions to optimize drug candidates and understand species differences across metabolite profiles in support of toxicology studies * Author reports, prepare data summaries and communicate results to project teams and management * Author regulatory submission documentation including IND summaries and Investigator Brochure * Mentor and motivate the in-house DMPK team What We Would Like to See: * PhD in Organic Chemistry, Drug Metabolism, Pharmacokinetics, Pharmaceutical Sciences, or related discipline with 7+ years of industry experience; MS/BS with 12+ years experience will also be considered * Expertise in drug metabolism, in vitro enzyme kinetics, ADME assays and LC/MS bioanalytical methodology * Experience in designing, executing and reviewing biotransformation studies * Understanding of regulatory guidance as it pertains to biotransformation including MIST * Experience in biotransformation document preparation for regulatory submissions is a plus Core Competencies: * Excellent written and verbal technical communication skills * Ability to lead, guide, and influence teams in decision-making * Collaborative team behaviors and ability to build and sustain relationships across internal scientific functions and the wider scientific community * Ability to work autonomously and collaboratively in a multidisciplinary team setting * Passion for data-driven analysis and strong business-of-science thinking * Ability to thrive in a fast-paced, highly matrixed environment * Strong understanding of DMPK, biotransformation, enzymology and DDI prediction strategies * Proven track record of leading studies to enable IND filing and contributions to drug discovery * Proficiency in managing CROs and robust knowledge of relevant regulatory guidance Further Information: In addition to a competitive compensation package with long-term incentives and 401k match, Vividion also offers a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, life, and disability insurance. Vividion Therapeutics, Inc. is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Privacy Policy: The protection of your personal information is a commitment we take seriously. For information regarding our Privacy Policy (CA candidates) please visit *************************************************************************

ElevateBio ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine. Our integrated technologies model offers turnkey scale and biotechnological capabilities to power genetic medicines processes, programs, and companies to their full potential. **The Role:** ElevateBio is looking for a Principal Associate Scientist to support the development and execution of novel molecular methods from the Analytical Development teams. The position will work closely with the AD SMEs, Analytical Testing Core and the QC team and will also participate in method optimization and lifecycle management of assays. This is a cross-functional role that will have the opportunity to impact numerous Cell and Gene therapy programs of Elevatebio. This is a four-month contract role. **Here's What You'll Do:** * Execute and support the development, optimization and execution of molecular assays in close collaboration with the Elevatebio Analytical Testing Core and QC team, for the characterization and testing of viral vectors (Lentiviral vector, AAV), cell and gene therapy products and critical components. * Collaborate with AD SMEs, Analytical Testing Core and the QC team to generate protocols, reports, other technical documents as part of test method development and optimization. * Communicate with key stakeholders to work through potential challenges, troubleshooting, during qualification and method transfer activities. * Provide necessary support during assay development as required. Participate in lifecycle management of assays, and implementation of new ideas and technologies. * Provide support during investigations of relevant deviation incidents related to assay qualification or validation efforts. * Analyze, interpret, and present data during team meetings and discussions. * Form active collaborations and communicate with teams within Analytical Development, Quality, and other functions as well as external vendors. **Requirements:** * BS or MS in cell biology, molecular biology, biochemistry, or related sciences with a minimum of 4 years (MS) or 6 years (BS) of relevant and progressive experience in a Biotech setting. * Experience in development/ qualification of analytical methods to QC GMP labs is preferred. Knowledge of ICH guidelines for method qualification/development is desirable. * Experience in a variety of molecular technologies, e.g., dd PCR, qPCR, ELISA, is required. * Knowledge or scientific background related to CGT products and viral vectors (e.g., Lentivirus, AAV) is a plus. * Must have strong writing, and communication skills. Must have prior experience of authoring and reviewing protocols and technical reports. * Good organization skills, multi-tasking, and ability to work in a cross-functional team environment is a must. ElevateBio is a technology-driven company built to power transformative genetic medicines today and for many decades to come. The Company commercializes its enabling technologies, manufacturing capabilities, and industry-leading expertise through partnerships to accelerate development across a breadth of therapeutic approaches and modalities. The ElevateBio ecosystem combines multiple R&D technology platforms - including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform - with BaseCamp , its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics. We aim to be the dominant engine inside the world's greatest scientific advancements harnessing human cells and genes to alter disease. **Our Mission:** To power the creation of life-transforming cell and gene therapies, at a speed the world deserves. **Our Vision:** We seek to be the world's most indispensable cell and gene therapy technology company, redefining how companies operate, how products are created and how disease is treated. *ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.*

**Job Type:** Full Time Remote **Education:** MS/MBA/Ph.D/PharmD/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science **Skills:** Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding ****Job Description: Associate Principal Scientist (Associate Director), Regulatory CMC**** **Organization:** Organon **Location:** Flexible Work Arrangements (Flex Time, Telecommuting) **Travel:** Up to 10% ****Position Overview**** The **Associate Principal Scientist (Associate Director)** is responsible for Regulatory Chemistry, Manufacturing, and Controls (CMC) activities for clinical-phase and market product registrations. This role ensures compliance with global regulations and oversees the regulatory CMC strategies for biological, biosimilar, and small molecule products, supporting Organon's focus on innovative women's health solutions. The incumbent collaborates with internal teams and external partners, including contract organizations, to achieve regulatory and business goals. ****Key Responsibilities**** ****Strategic Leadership**** * Develop and execute **Regulatory CMC strategies** for late-stage development, commercial, and licensed products, ensuring compliance with global regulations and guidance. * Lead the preparation and authoring of regulatory submissions, including IND/CTA, NDA/BLA, and post-approval documentation. * Provide input for **Health Authority engagement**, including strategy, background packages, and participation in CMC-related meetings. ****Regulatory Compliance and Documentation**** * Ensure submissions meet regulatory requirements, timelines, and e-publishing standards. * Oversee quality and technical congruency of regulatory CMC content, ensuring accuracy and regulatory compliance. * Assess CMC changes during development and define global regulatory requirements while balancing risk and opportunity. ****Collaboration and Stakeholder Management**** * Partner with internal teams (Research & Development, Manufacturing & Supply, Business Development, and Commercial) and external partners to align strategies and deliverables. * Embed regulatory CMC activities into product development plans, providing a clear roadmap for approvals and robust supply chains. ****Risk and Issue Management**** * Identify, communicate, and escalate potential regulatory issues to Organon Regulatory CMC leadership. * Evaluate technical documentation for completeness and suitability, leveraging regulatory intelligence to address challenges effectively. ****Continuous Improvement and Leadership**** * Contribute to organizational initiatives and process improvements, focusing on efficiency and agility in regulatory CMC operations. * Provide mentorship and leadership to matrixed teams, ensuring alignment with project timelines and business objectives. ****Required Education, Experience, and Skills**** ****Education**** * Bachelor's degree in a science, engineering, or related field (e.g., Pharmacy, Chemistry, Chemical Engineering, Biology, Microbiology, Molecular Biology, Biochemistry). + **Experience Required:** At least **7 years** of relevant experience. * Advanced degree (MS, MBA, Ph.D., PharmD) preferred. + **Experience Required:** At least **5 years** of relevant experience. ****Core Competencies**** * **Regulatory Expertise:** Strong understanding of global regulatory CMC guidelines and post-approval change management. * **Technical Proficiency:** Skilled in authoring and reviewing regulatory documentation, ensuring clarity and data-supported conclusions. * **Communication Skills:** Exceptional oral and written communication, with the ability to address complex issues succinctly. * **Cross-Disciplinary Knowledge:** Knowledge of pharmaceutical manufacturing, process development, analytical testing, and quality assurance. ****Leadership and Project Management**** * Proven ability to manage multiple projects, deliver on commitments, and meet timelines. * Demonstrated flexibility in addressing changing priorities and unexpected events. * Experience in leading teams and collaborating across multicultural and matrixed settings. ****Preferred Skills and Experience**** * **Regulatory CMC Specialization:** Direct experience with biologics, biosimilars, and device/combination products. * **Technical Problem-Solving:** Innovative approaches to complex regulatory challenges. * **Advanced Communication Skills:** Superior ability to communicate across diverse audiences and cultures. * **Device Experience:** Regulatory expertise in combination products and devices. ****About Organon**** Organon is a global leader in healthcare solutions, focused on women's health and expanding access to trusted health products, biosimilars, and innovative therapeutics. We strive to create a better and healthier future, fostering an inclusive and collaborative environment where everyone can excel. ****Employment Details**** * **Status:** Regular * **Relocation:** Not available * **Visa Sponsorship:** Not available * **Work Arrangements:** Flex Time, Telecommuting Organon embraces diversity and equal opportunity, ensuring that all employees and applicants are treated equitably without regard to race, gender, age, or other protected characteristics. For more information about your rights under Equal Employment Opportunity, visit: * EEOC Poster * EEOC GINA Supplement **Salary Range (US):** $124,000 - $210,700 *Salary ranges vary by location.* For additional information, visit Organon Careers.

At RefinedScience, our mission is to advance care by bringing together the best science, data and minds - disease by disease, patient by patient, cell by cell to discover pathways to life beyond disease. WHAT WE ARE LOOKING FOR RefinedScience is seeking Scientist I to join an interdisciplinary team of computational biologists, data scientists, data engineers, cancer biologists, and clinicians who are seeking to develop new therapies, diagnostics, clinical decision support tools and optimize clinical trials for cancer and other diseases. KEY ACTIVITIES * The Scientist I will work directly with the Director, Translational Laboratory Research, CTO, CINO performing a wide range of cutting edge experiments to characterize specimens from patients to develop new therapies, diagnostics, clinical decision support tools and optimize clinical trials for cancer and other diseases. * Utilize a variety of laboratory techniques required for research projects to perform experiments and tabulate and analyze research with below techniques: + Isolation of rare blood and blood progenitor cells from bone marrow using magnetic bead separation and flow cytometry + In vitro functional assays on human cells; maintenance of cell cultures + Primer design and DNA/RNA manipulation + Quantitative PCR + Molecular cloning + High throughput DNA sequencing + Single cell technologies including library construction, quantification, and sequencing workflows + Gene expression studies, including RNAseq and RNAi technology * Provide laboratory science expertise and leadership in study design, study oversight, data management, data analysis and manuscript preparation to assist all levels of investigators, and researchers on new research activities across a wide range of disciplines * Teach staff as needed, review relevant scientific literature, and attend and present at lab meetings * Provide oversight on reagent purchases through management of budget and tracking of spending on specific projects, requiring in depth knowledge of nature of each individual project. Included in this duty is preparing a report of spending on projects and working with closely with administrative team to align budgets and spending. * Assist with identifying issues related to operational efficiency and shares results with leadership * Serve as a resource to PIs and other stakeholders * Independently and creatively identify laboratory solutions * Independently review, develop and implement new or modified laboratory techniques required for research projects * Assist management with creation and implementation of processes and procedures and quality improvement initiatives * Prepare lab for daily operations, including ordering, inventory, cleaning, and preparation of laboratory reagents * Pick up, transport, and maintain results, samples, documents, materials and other items as needed * The candidate will serve as lead on many of the above tasks including oversight and providing informal leadership to team members, including assistance in managing day-to-day priorities, and redistributing workloads, and mentoring staff. Will also lead in the identification of training and development opportunities for new and existing team members MUST HAVES * BS, MS, and/or PhD in Immunology, Molecular Biology, Cell Biology, or in a related discipline * BS with 7+ years experience in a lab setting, MS with 3+ years, or PhD with 1+ years experience in a lab setting, either within an industry and/or academic setting NICE TO HAVES * Prior experience with cancer therapeutics, drug and clinical trial development. * Prior experience with single cell technologies, flow cytometry, and working with human cells and tissues * Familiarity with bioinformatics (i.e., computational, molecular, and cellular biology). * Familiarity with quality assurance principles and activities (e.g. QMS), regulatory requirements (e.g., GDPR, HIPAA), and project management principles and tools (e.g., PMO, Slack, JIRA). WHY YOU'LL LOVE REFINED SCIENCE **Team + Values** At RefinedScience, we seamlessly integrate top-tier clinical and biological data with expert knowledge to provide unparalleled insights. We maximize patient impact with these unique insights by optimizing clinical trial probability of success and time to actionable results. We work across biopharma and we are a trusted partner in achieving better results, faster - working together to unlock strategic advantage. **Our Values** * Act with Purpose - We believe in rigor through deliberate and thoughtful actions * Be Curious - Curiosity is the spark that ignites innovation and growth * Take Ownership - True ownership leads to pride and commitment in the work we do * Invest in Relationships - Building strong connections is the foundation for effective collaboration and trust for long term success * Embrace Agility - We celebrate agile thinking, resilience, and adaptability WHAT WE OFFER * The target salary range is $70,000 - $90,000 per year * Base pay offered may vary within the posted range based on several factors, including but not limited to education, job-related knowledge, skills, experience, and location.

CBD Living Water is seeking an experienced, formulation scientist. The position requires someone with a strong work ethic, looking to make a long-term commitment to the company. Our products are made in our state of the art laboratory and include CBD infused beverages, tinctures, personal care items, confectioneries, and pet care items. Responsibilities Formulate CBD infused products by following Standard Operating Procedures Develop innovative new products and draft Standard Operating Procedures Communicate with third party analytics laboratories and interpret all results Use in-house analytics equipment for QA/QC purposes (including gas chromatography, UV-vis Spectroscopy and Dynamic Light Scattering) Required Experience Experience in cannabis, pharmaceutical, or food industry desired Professional or educational laboratory experience Preferred Skills Emulsions and nanotechnology Direct compression tablet production Food safety Laboratory calculations Required Education BS, MS, or PhD in physical or life sciences OR Equivalent laboratory and formulation experience **Compensation based upon education and experience Please send a resume AND cover letter. No applications without a cover letter will be considered. You may choose to also send a CV of relevant coursework but are not required to. Job Type: Full-time Salary: $40,000.00 to $90,000.00 /year Job Description CBD Living Water is seeking an experienced, formulation scientist. The position requires someone with a strong work ethic, looking to make a long-term commitment to the company. Our products are made in our state of the art laboratory and include CBD infused beverages, tinctures, personal care items, confectioneries, and pet care items. Responsibilities Formulate CBD infused products by following Standard Operating Procedures Develop innovative new products and draft Standard Operating Procedures Communicate with third party analytics laboratories and interpret all results Use in-house analytics equipment for QA/QC purposes (including gas chromatography, UV-vis Spectroscopy and Dynamic Light Scattering) Required Experience Experience in cannabis, pharmaceutical, or food industry desired Professional or educational laboratory experience Preferred Skills Emulsions and nanotechnology Direct compression tablet production Food safety Laboratory calculations Required Education BS, MS, or PhD in physical or life sciences OR Equivalent laboratory and formulation experience **Compensation based upon education and experience Please send a resume AND cover letter. No applications without a cover letter will be considered. You may choose to also send a CV of relevant coursework but are not required to. Job Type: Full-time Salary: $40,000.00 to $90,000.00 /year

As required by our governmental client, this position requires being a US Citizen, lawful resident alien, citizen of American Samoa or other territory owning permanent allegiance to the United States. As an analyst for the military drug testing community and the Armed Forces Medical Examiner, conduct analyses on biological specimens, offering screening, confirmation, and quantitative data. Provide full scan mass spectra, implement corrective actions, and contribute to SOP revisions, updates, and improvements for the post-mortem laboratory's daily operations. Additionally, support research and analytical projects as assigned. **Compensation & Benefits:** * Pay commensurate with experience. * Full time benefits include Medical, Dental, Vision, 401K and other possible benefits as provided. * Benefits are subject to change with or without notice. **Analytical Toxicologist II Responsibilities Include:** * Conduct analyses on biological specimens for the military drug testing community and the Armed Forces Medical Examiner. * Provide screening and confirmation data for identified substances. * Analyze and report quantitative data related to drug testing results. * Generate and interpret full scan mass spectra to identify and characterize compounds. * Implement corrective actions to address any issues identified during analyses, ensuring accuracy and reliability. * Contribute to the revision, updating, and improvement of Standard Operating Procedures (SOPs) for the post-mortem laboratory. * Support the daily operation of the post-mortem laboratory, ensuring efficiency and adherence to established protocols. * Assist in research initiatives and analytical projects as assigned, contributing to advancements in the field. * Performs other job-related duties as assigned. **Analytical Toxicologist II Experience, Education, Skills, Abilities requested:** * A minimum of a Bachelor's degree in Analytical Chemistry, Toxicology, Pharmacology, or a closely related field. Advanced degrees (Master's or Ph.D.) may be preferred. * Typically requires 2-5 years of relevant experience in a laboratory setting, with a focus on analytical toxicology. * Proficiency in advanced analytical techniques and instrumentation commonly used in toxicology, such as gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS). * Hands-on experience in conducting complex toxicological analyses on various specimens, including biological fluids and tissues. * Understanding of and experience with regulatory requirements and guidelines related to toxicology, including familiarity with forensic and clinical toxicology procedures. * Experience in quality assurance practices within a laboratory setting to ensure accuracy and reliability of results. * Strong communication skills for effectively reporting findings, collaborating with interdisciplinary teams, and potentially providing expert testimony. * Demonstrated experience in a laboratory environment, with a focus on conducting advanced toxicological analyses and interpreting complex results. * Proven expertise in utilizing a range of advanced analytical techniques and instrumentation specific to toxicology. * Experience in forensic toxicology, including providing screening and confirmation data for investigations. * Previous involvement in managing and overseeing toxicology projects, ensuring timely and accurate completion. * Experience contributing to research projects, publications, or advancements in the field of toxicology. * Must pass pre-employment qualifications of Cherokee Federal. **Company Information:** **Cherokee Nation Integrated Health (CNIH)** is a part of Cherokee Federal - the division of tribally owned federal contracting companies owned by Cherokee Nation Businesses. As a trusted partner for more than 60 federal clients, Cherokee Federal LLCs are focused on building a brighter future, solving complex challenges, and **serving** the government's mission with compassion and heart. To learn more about **CNIH**, visit cherokee-federal.com. **#CherokeeFederal #LI** Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply. Similar searchable job titles * Senior Analytical Toxicologist * Lead Forensic Toxicologist * Analytical Toxicology Supervisor * Principal Toxicologist * Toxicology Laboratory Manager Keywords 5 times * Advanced toxicological analysis * Expertise in analytical techniques * Forensic toxicology experience * Laboratory supervision * Regulatory compliance in toxicology **Legal Disclaimer:** Cherokee Federal is an equal opportunity employer. Please visit cherokee-federal.com/careers for information regarding our Affirmative Action and Equal Opportunity Employer Statement, and Accommodation request. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. **Please Note: This position is pending a contract award. If you are interested in a future with Cherokee Federal, APPLY TODAY! Although this is not an approved position, we are accepting applications for this future and anticipated need.**

We are hiring for a Scientist to incorporate to our Elemental Analysis department. The person Will be assigned the following responsibilities: * Management and execution of ICP-MS and AAS studies that are carried out for Quality Control and Stability Studies of pharmaceutical, veterinary, health and cosmetic products. * Management, execution and review of tests by ICP-MS and AAS for development studies, validation and / or method transfers and routine sample analysis. * Design, supervision, review and execution of method validation by ICP-MS and AAS. * Drafting and review of related documentation (SOP, protocols, guides, reports, etc.). * Direct involvement in all technical aspects related to analytical methods, problem solving, transfer of analytical methods, etc. * Management and writing of Incidents, deviations, OOS and CAPAs. * Management and organization of the qualification of the teams assigned to the department. * Management of studies and results through LIMS system. * Contact with the Quality Control and Stability departments of the company * Work under GMP and GLP compliance. We are looking for a candidate with: * University degree: Chemistry or Pharmacy Bachelor's. * Some experience in a Quality Control department in the Pharmaceutical industry or Third-Party Analysis Company (CRO). * Experience in management, design and performance of physicochemical tests of active ingredients, drugs, cosmetics, ... * Experience in working with computerized systems. * Experience in working under GMP and GLP standards. * Knowledge of pharmacopoeias, guidelines, regulations that apply in the field of GMPs. * Advanced English level is a must. * Knowledge of the ICH Q3D guideline will be valued.

Rockville, Maryland Operations - Bioanalytical Sciences / Full Time / On-site + Develops, qualifies and/or validates robust bioanalytical methods per Health Authority Guidance Documents using Mass Spectrometry platforms to support the Company pipeline. + Promotes innovation and direct operational improvement and/or evaluation of new analytical techniques or technology. + Troubleshoots and resolves bioanalytical method issues to successful resolution. + Takes accountability and demonstrates responsibility regarding scientific study conduct. + Ensures analytical development/validation activities conducted internally and with contracted services lead to robust methods that support bioanalytical analysis. + Conducts technology transfer between research organization, in-house and contract laboratories. + Serves as the Responsible/lead Scientist for the bioanalytical portion of non-regulated as well as GLP and GCP studies. + Writes and reviews study protocols, analytical procedure, reports for regulatory submissions. + Performs technical reviews of analytical data and be responsible for data interpretation, analysis, and reporting of results for method development and validation. + Provides scientific and technical input to the study team and other departments. + Ensures that any circumstances that may affect the quality and integrity of the study are identified and documented as they occur and that appropriate corrective actions are taken. + Identifies process improvement opportunities, participates in execution of initiatives. + Coordinates parallel tasks across multiple projects and plans, prioritizes, and manages duties to meet departmental and organizational goals. + Mentors and/or trains new and less-experienced employees and develops training materials and schedules. + Reviews and participates in writing of departmental Standard Operating Procedures (SOPs). + Performs additional tasks or assist with special projects as assigned or needed. + The Scientist will be required to maintain familiarity with scientific literature and apply it appropriately to projects (such as evaluating new methodologies and techniques) **We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications:** + PhD in relevant scientific discipline with 2-5 years of industry or post-doctoral experience or Master's degree in relevant scientific discipline with 5+ years of relevant experience + Solid understanding of Mass Spectrometry platforms and working knowledge of Sciex instruments (7500 Triple Quad preferred).. + Knowledge/hands-on experience with LBA and/or qPCR/dd PCR methods is a plus + Working knowledge of relevant bioanalytical FDA guidance documents and health authorities expectations of bioanalytical assays. + Ability to independently plan experiments, willingness to solicit feedback and guidance to ensure proposals align with project needs + Ability to perform and execute experiments in a timely fashion to support scientific activities and project goals/deliverables + Ability to develop a wide range of methodologies/technologies and perform advanced data analysis + Ability to recommend alternatives as well as research new methods and techniques + Demonstrated ability to analyze and resolve problems, troubleshoot assay issues + Ability to interpret data, draw conclusions, and recommend next steps + Ability to effectively communicate information and results in the appropriate format (i.e. lab notebooks, presentations, reports, etc.) + Ability to lead internal and external functional projects + Must possess excellent oral and written communication skills. + Ability to present technical information to both technical and non-technical audience is required + Ability to effectively communicate information and results in the appropriate format (i.e. lab notebooks, presentations, etc.) + Must be able to work collaboratively and effectively as part of a team + Prior industry experience preferred + Familiarity with statistical analysis tools and able to apply the basic statistic tools desired. + Good computer skills and working knowledge of SoftMax or other data analysis software, MS word, Excel, Power Point are required. + Knowledge of gene therapy is a plus. **Why You Should Apply** By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. In addition, professional development is important to us. By joining our team, you'll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally. We are proud to offer a comprehensive rewards package which includes a market-competitive base salary, an annual performance-based bonus program, stock grants at all levels, and benefits such as health, dental, and vision insurance, retirement plan with 401(k) match, summer hours, and more! The estimated compensation range for this role is $98,000 to $133,000 annually. The actual salary offered to the final candidate depends on a number of factors such as relevant work experience, skills, education, and years of experience.

Sr. Scientist, TS/MS - Parenteral page is loaded **Sr. Scientist, TS/MS - Parenteral** **Sr. Scientist, TS/MS - Parenteral** locations US, Concord NC time type Full time posted on Posted 30+ Days Ago job requisition idR-71343 At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism. Lilly unites caring with discovery to create medicines that make life better for people around the world. Lilly is a fortune 500 company that has been in operation for over 140 years. We make medicine with safety first and quality always while living our company values of Integrity, Excellence, and Respect for People. Lilly is designing and building a new state of the art Parenteral, Device Assembly, and Packaging Facility located in Concord, North Carolina. This is an exciting opportunity to help build and operate a state-of-the-art manufacturing site and Quality System from the ground up. The Scientist within the Concord TS/MS Parenteral process team is a position supporting the implementation of technical objectives through execution activities and partnership with the parenteral operations and engineering teams. This role will initially supplement the delivery of formulation, filling, and inspection lines and serve as technical resource for internal parties. Upon the start of commercial production, this role's objectives include analyzing equipment/process data, monitoring production metrics, authoring and executing protocols, and serving as a technical asset for process improvement and root cause investigations. This role is expected to interface regularly with the parenteral operations and engineering teams in support of day-to-day operations. **Responsibilities:** * Support the Parenteral Process Team as TS/MS representative. * Provide technical support to non-routine (e.g., deviation, complaint) investigations, including consultation on quality and stability issues. * Prepare and Review, as required, relevant technical documents, such as: Change Controls, Regulatory Submissions, Deviations, Validations, Protocols, Procedures, PFDs, pFMEAs, etc. * Provide technical support for non-routine (e.g., deviation, complaint) investigations, including consultation on quality and product impact. * Identify opportunities and participate in projects to improve process control and/or productivity. * Serve as floor-level support and technical interface for parenteral components, equipment, and operations for the TS/MS team. **Basic Requirements:** * Bachelors or equivalent (Science or Engineering related degree preferred) **Additional Preferences:** * Pharmaceutical and/or medical device manufacturing experience * Root cause investigation experience * Proven ability to work independently or as part of a team to resolve an issue. * Strong attention to detail. * Proficiency with computer systems including Microsoft Office products, Veeva Vault, TrackWise, electronic batch records, and SAP. * Knowledge and understanding of manufacturing processes * Strong interpersonal and teamwork skills * Strong self-management and organizational skills **Additional Information:** * Role is Monday through Friday. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and /or off-hour work may be required. * Position will be based out of Concord, NC site with ability to travel to Indianapolis and other global Lilly sites as required. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form () for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups. #WeAreLilly locations US, Concord NC time type Full time posted on Posted 30+ Days Ago At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!

**Scientist - DNA-, RNA- Oligonucleotide Synthesis (x/f/m)** * Full-time * Department: Scientific / Technical Science ** Axolabs specialises in a new class of drugs whose active ingredients are chemically derived from DNA or RNA. They are called oligonucleotide or nucleic acid therapeutics. We use our many years of expertise to help our clients make them a success. Some of these drugs have already been approved and are being used successfully against diseases that were previously untreatable in some cases. New drugs from this class are added every year. We believe in Science for a Safer World and are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization. LGC Axolabs is located in Petaluma, US, Kulmbach and Berlin, Germany. **Job Description** **Join Our Innovative R&D Team in Oligonucleotide Chemistry!** **Your Key Responsibilities** * Develop innovative synthetic and downstream processing routes for complex oligonucleotide formats, including conjugates with fatty acids, peptides, and antibodies * Collaborate with the team to design and execute experiments that optimize lead oligonucleotide drug candidates, focusing on potency, selectivity, stability, and pharmacokinetic properties * Take on responsibility for customer order projects after a thorough training period * Support the Department Head in project planning, client communication, and report writing * Analyze experimental data, interpret results, and present findings internally, to customers, or at international conferences. Contribute to technical reports and manuscripts for publication in peer-reviewed journals * Guide and coach junior staff members in the oligonucleotide synthesis laboratory **Qualifications** **Education & Preferred Qualifications** * Hands-on experience in oligonucleotide synthesis via automated solid-phase methodologies, complemented by a Ph.D. in Chemistry or Biochemistry, or equivalent experience * Prior experience in ligation chemistry (enzymatic and/or chemical) is required * Proficient in conjugation and purification technologies, with expertise in HPLC, LC-MS, UV spectroscopy, and endotoxin measurement and control * Strong oral and written communication skills in English, ideally also in German, with a keen ability to maintain detailed lab notebooks and reports * A reliable, dedicated working style characterized by a focus on quality, dedication, and excellent communication skills **Your benefits** * Comprehensive onboarding and mentoring for a successful start * Permanent employment contract * Responsible tasks and individual development and career opportunities in an innovative, international company * An open corporate culture that values integrity, respect, and a passion for forward-thinking, creative solutions * Company pension scheme and attractive employer subsidies, such as JobRad, as well as corporate benefits * Extensive employee offerings related to health management, as well as online options for childcare and educational support * 30 days of annual leave * Relocation assistance for candidates from outside the region * 100% coverage of the Jobticket (Deutschlandticket) or a free parking space in the adjacent parking garage Join our innovative team and be part of the exciting future of oligonucleotide research! We look forward to receiving your application **in English**. **Additional Information** **ABOUT LGC:** LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality, and range. **OUR VALUES** **Passion** for our work makes the world a safer place. We are inspired by our purpose. It drives us forward to deliver the best we can every day. **Curiosity** makes tomorrow's innovations possible. We challenge and question to discover creative and innovative solutions, enabling our customers and LGC to grow and evolve. **Integrity** is embedded in LGC and our 180+ year heritage. We hold ourselves to the highest standards and trust our colleagues to do the right thing. **Brilliance** is in everything we do. Our remarkable colleagues are experts in their field. They collaborate to deliver brilliant science to exceed our customers' expectations. **Respect** for individuality and diversity is our strength. We respect and value our colleagues, our customers, our environment and our science. **EQUAL OPPORTUNITIES** LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. For more information about LGC, please visit our website **#scienceforasaferworld** **Job Location** Scientist - DNA-, RNA- Oligonucleotide Synthesis (x/f/m) * Fritz-Hornschuch-Straße 9, 95326 Kulmbach, Germany * Full-time

Share **Scientist- Bioanalysis (LC-MS/MS)** Full-time Regular Dir= 100% / OH= 0% 3 days ago Requisition ID: 1445 At ITR Laboratories Canada INC Our Mission is to bring new medicines to the world which relieve patients suffering from serious diseases. ITR Laboratories Canada has been servicing the pharmaceutical and biotechnology industries for over 30 years and has established itself as a trusted partner worldwide in Drug Safety Testing. We are actively seeking a **Scientist- Bioanalysis (LC-MS/MS)** to join our team as we continue to expand our reach and services. **Responsibilities:** The Scientist will be experienced in research and development for Bioanalytical LC-MS/MS assays. They will need to develop innovative solutions to mass spectrometry challenges. They will troubleshoot, optimize and develop assays to current GLP regulatory requirements. **Tasks Performed:** * Strong understanding of LC-MS/MS theory and applications. * Experienced in serum/plasma and tissue sample extraction techniques. * Research and development for LC-MS/MS assays including troubleshooting ongoing assays. * Conduct analytical pre-clinical and clinical studies in compliance with the Study Plan/Amendments, GLPs, SOPs, and current industry best practices. * Provide research project planning and deliver on time solutions. * Interpretation, analysis, documentation, and reporting of results on Analytical projects (validation and sample analysis). * Co-ordinate results with various Clients, Consultants and Toxicology Study Directors. * Generate reports, or reporting of results, within study timelines, and ensure any deviations/exception events are acceptable, including their impact on study data. * Keep up to date with respect to pertinent regulatory developments in the industry. * Write, review and apply all relevant SOPs. **Qualifications :** * Masters of Science (Chemistry, Biochemistry, Biotechnology, Pharmacology or related field). * Scientific industry experience of project management. * Excellent understanding of bioanalytical analysis and the associated regulations. * Experience and good hands on knowledge of analytical instrumentation (LC-MS/MS). * A strong team player with excellent oral and written communication skills. * Skilled in data interpretation and report writing. * Bilingual English /French; **This position offers:** * Permanent full-time position, * Group insurance plan and group RRSP. * A stimulating and friendly work environment. Start Date: ASAP

NameProviderPurposeExpiryTypeNameProviderPurposeExpiryTypelidcRegisters which server-cluster is serving the visitor. This is used in context with load balancing, in order to optimize user experience. 1 day HTTPNameProviderPurposeExpiryTypeNameProviderPurposeExpiryTypeNameProviderPurposeExpiryType **MSAT Scientist** **Geel*I*Pharmaceutical Sector** Job description At the moment we're looking for a **MSAT Scientist** to reinforce our team in Geel. You will be responsible for the development, execution, and transfer of liquid-chromatography coupled to mass spectrometry (**LC-MS**) methods. Acting as an expert in LC-MS and analytical high-performance liquid chromatography (**HPLC**), you will integrate characterization LC-MS data with process and product knowledge. Key Responsibilities: * Develop, execute, and transfer LC-MS methods for various analytical purposes * Serve as an expert in LC-MS and analytical HPLC techniques, providing guidance and support to the analytical team * Integrate LC-MS data with process and product knowledge to enhance understanding and drive improvements * Take ownership of methods from development through validation and transfer, ensuring robustness and reliability * Identify opportunities for method improvements, introducing new technology, enhancing robustness, and reducing release cycle time * Provide investigational support for product and process issues, including the generation of scientific/technical study protocols and reports * Assess the impact of significant deviations in analytical methods or production processes, offering technical and scientific expertise to address issues effectively * Support analytical activities for product characterization, transfer, and process improvements across various developmental stages, from late development to commercialization Profile * You have a **PhD or Master in Life Sciences** or equivalent through relevant experience * Prior hands-on experience with LC-MS is highly desired * You speak fluently **Dutch and English** Organisation and department description At **Select Projects**, the customer's experience with our staff is key. It is our consultants who ensure an optimal experience by delivering the highest quality. Your professionalism is central to this and you can continue to grow at **Select Projects** **Select Projects** offers substantively interesting projects, growth opportunities, autonomy, trust, training courses and expert colleagues you can learn from. This allows you to work fully on your professional growth and personal development. At **Select Projects**, you are not only part of the team at the customer's site. You will also form a team with your fellow consultants in the field. We have family values where we help each other and pay attention to each other. This allows you to become and give the best version of yourself. Working at **Select Projects** means working on your craftsmanship and therefore being the specialist in your field.Offer Select Projects ensures that you end up in a **pleasant working environment** with fun colleagues where team spirit is key. We organise after-works, staff parties, sports events, team building, etc. We offer you opportunities to develop and evolve. Together with you, we map out a **training programme** tailored to your future plans and needs. At Select Projects, you can become and give the best version of yourself. In addition, Select Projects offers you a **permanent contract** of undetermined duration. You receive an **attractive salary** package including the following **additional benefits**: * Possibility of a **company car** with fuel card * Meal & eco vouchers * Expense allowance * Group & hospitalisation **insurance** * 12 ADV-days on an annual base * End-of-year bonus * Single and double holiday pay * **Bonus system**: collective bonus and individual bonus * Possibility to participate in Flex Income Plan MSAT Scientist Vacancy information

**Our Company** Gentuity is an exciting and highly innovative medical technology firm, active in the research and development, clinical translation, and commercialization of vascular imaging devices. This opportunity provides the candidates the unique chance to work on innovative medical products, with the potential to significantly change the practice of medicine in the care of patients suffering from a wide range of highly debilitating vascular diseases. **SUMMARY OF PRIMARY DUTIES AND RESPONSIBILITIES:** * Experiment with state-of-the-art methods in camera-based 2D/3D segmentation, inter-modality co-registration, object detection and classification of key features within the IV-OCT imaging data. * Train neural networks on large-scale in-house OCT and X-ray Angiogram datasets. * Analyze experimental results and come up with ways to improve the accuracy and scalability of our models. * Help integrate models into the Gentuity system software, including profiling and optimization of both the model and the end-to-end AI pipeline. * Collaborate with researchers and engineers across several organizations within the company. **EXPERIENCE/SKILL REQUIREMENTS:** * 5+ years of relevant work experience with MS OR 2+ years of experience with PhD (postdoc included) * Extensive experience with Deep Learning, Computer Vision or a related field. * Advanced AI/ML experience in foundational models, generative AI, multi-modal models, multi-instance learning, semi/weakly/un-supervised learning and other cutting-edge ideas. * Experience with deep neural network training in leading frameworks such as TensorFlow and/or PyTorch. * Solid fundamentals in computer vision and ML theory. **EDUCATIONAL REQUIREMENTS:** * MS, or PhD degree in Engineering or Computer Science or equivalent experience. ** Machine Learning Scientist** **Department** Software **Employment Type** Full Time **Location** Sudbury

Join world-class R&D team as we work to reshape the future of health diagnostics. We are on a mission to extend and enhance life by developing non-invasive biometric testing, driven by groundbreaking AI technology. By joining us, you'll be at the forefront of healthcare technology, innovation and research. Your work will make a tangible difference to people's lives as we follow our journey from radical vision to transformative reality. ****What the role involves**** You will be working directly with our Chief Science Officer, helping to drive forward our efforts to identify and quantify compounds in breath and other biological materials. Key aspects of the role will include: * Develop, optimize and validate analytical methods using LC-MS, SESI-HRMS and other modes of sample delivery to identify and quantify metabolic compounds and exogenous compounds * Design and implement bench-scale experiments with multiple variables for small molecule compounds * Collaborate cross-functionally with others in the R&D team and wider company ****What we are looking for**** We are looking for a skilled researcher to join our growing team of scientists and engineers. The ideal candidate will display the following attributes: * Able to communicate clearly with people who have little or no knowledge of mass spectrometry and metabolomics * Able to maintain an excellent laboratory notebook * Able and willing to mentor junior team members * Prepared to voice ideas, discuss concerns, and offer solutions when engaging with others * Able to cope with the rapidly changing priorities that come with working in a startup environment * Being able to work in a startup environment which comes with shifting priorities. ****Required skills and experience**** We want candidates with the following experience: ****Essential**** * Ph.D. degree in Analytical Chemistry, Chemistry, Biochemistry or related fields * Experience using the Thermo Scientific Q-exactive platform, including data analysis using both Thermo software and open-source software * Experience with Fossilion Tech SESI devices * Proficiency in untargeted and targeted metabolomics and lipidomics data processing, statistical analysis and data interpretation * Ability to run LC-MS experiments without supervision * Knowledge of instrumentation hardware and software * Willing to relocate to San Francisco Bay Area ****Desirable**** * 5+ years of laboratory (academic and/or industrial) experience developing analytical methods for small molecule analysis (LC, MS, GC) * Proficiency using Python based analysis tools is desirable * Strong problem-solving skills and proven creativity * Strong oral and written communication skills * Proven ability to work effectively within a diverse and dynamic team * Start-up company experience is a plus ****What we offer**** The successful candidate will get * A good salary (range $120k-160k) * A competitive compensation package including medical/dental care, 401K, paid time off, holidays, and share options. * A generous relocation package where relevant. * The chance to work in a cutting edge lab in the heart of San Francisco's Bay Area We also offer assistance with visa applications and Physical Requirements ****Equal opportunities**** Diagnose Early is an equal opportunity employer. This role is FLSA exempt. ****Note**** This role involves the following physical activities: standing, sitting, walking, climbing stairs, light lifting, computer operation, operation of analytical equipment.

At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs, but few options. **Who We Are:** **What We Do:** Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine, and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit , and follow the company on , and . (**in collaboration with AbbVie*) **About the Role:** The Sr. Principal Scientist/Assoc. Director, Antibody Engineering will lead laboratory activities related to antibody engineering including library construction, affinity optimization, and developability engineering. The ideal candidate will have extensive hands-on experience and a proven track record in therapeutic antibody optimization, in a biotechnology or pharmaceutical company setting. The person in this role will support early-mid stage protein engineering in all therapeutic areas of Neurocrine's biotherapeutic pipeline.\_ **Your Contributions (include, but are not limited to):** * **Neurocrine is further expanding its team of scientists with proven track records, to drive therapeutic pipeline progression from discovery to lead selection within a cutting-edge antibody engineering team** * **We are seeking a lead protein engineer responsible for all aspects of construct design, molecular cloning, multi-piece DNA assembly, site-directed mutagenesis, and preparation of libraries** * **Responsibilities include generating and screening site-directed, CDR randomization and combinatorial antibody libraries for affinity maturation and developability optimization** * **A critical member of the team contributing to characterizing antibodies and antibody-based therapeutics (e.g. affinity, specificity, cross-species binding, epitope determination)** * **Will be involved in the engineering of advanced modalities such as muti-specific antibodies and antibody conjugates** * **Experience with the design and cloning of antigens for immunization and screening** * **Familiarity with structural modeling software such as PyMol or MOE and experience using antibody structure to help mitigate developability issues** * **Responsible for understanding experimental data from multiple sources, forming hypotheses, devising strategies, and implementing prioritization to drive projects** * **Contribute to the evaluation of emerging molecular biological or biochemical methods, initiate and support new platforms, instrumentation, and technologies related to antibody engineering** * **Work cross-functionally with protein biochemists, cell biologists, and gene therapists to achieve project goals** * **Other duties as assigned** **Requirements:** * **PhD in Molecular Biology, Biochemistry, or other relevant discipline and 15+ years of relevant experience in the Biopharma industry** * **Knowledgeable in myriad aspects of antibody structure/function including developability screening, effector function (ADCC, ADCP, CDC, and cell-based reporter assays), half-life extension strategies, immunogenicity assessment, and bispecific formats** * **Hands-on experience in the design and execution of antibody optimization campaigns using directed evolution screening platforms such as capture-lift, phage display, or yeast display** * **Demonstrated mastery of standard molecular biology bench skills, DNA sequence analysis and software, and oligo design coupled with a strong desire to optimize laboratory practices** * **Experience building, training, and leading a team of productive bench scientists** * **Experience with standard laboratory instrumentation: PCR, centrifugation, DNA quantitation, gel documentation systems, plate readers and washers, liquid handling, etc.** * **Familiarity with affinity determination methods (e.g. ELISA, MSD, Octet, Carterra, Biacore, or Kinexa)** * **Ability to maintain detailed experimental documentation using Benchling** * **Excellent communication and interpersonal skills with an ability to work both independently and in a team environment** * **Proficiency in Microsoft Office and DNA sequence analysis software such as Sequencher, Geneious, SnapGene** * **Experience with various antibody formats including Fab, sc Fv, IgG, nanobody, conjugates, and multi-specific derivatives** * **Knowledge of standard antibody assay and cloning reagents and preferred vendors** * **Experience working with CROs for antibody discovery, expression, purification, and characterization** **#LI-AD1** Neurocrine Biosciences is an EEO/AA/Disability/Vets employer. We are committed to building a diverse, equitable, and inclusive workplace, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description. \_ The annual base salary we reasonably expect to pay is $150,700.00-$218,500.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.