Principal research scientist jobs in Colorado

-Lead, collaborate, and execute on research that pushes forward the state of the art in multimodal reasoning and generation research.-Work towards long-term ambitious research goals, while identifying intermediate milestones.-Directly contribute to experiments, including designing experimental details, writing reusable code, running evaluations, and organizing results.-Work with a large team.-Contribute to publications and open-sourcing efforts.-Mentor other team members. Play a significant role in healthy cross-functional collaboration.-Prioritize research that can be applied to Meta's product development. **Required Skills:** AI Research Scientist, VLLM (vision large language models) Responsibilities: 1. Push state of the art in multimodal generative AI 2. Explore new techniques for advanced reasoning and multimodal understanding for AI Assistants 3. Mentor and work with AI/ML engineers to find a path from research to production **Minimum Qualifications:** Minimum Qualifications: 4. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience 5. A PhD in AI, computer science, or related technical fields 6. Publications in machine learning, computer vision, NLP, speech 7. Experience writing software and executing complex experiments involving large AI models and datasets 8. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment **Preferred Qualifications:** Preferred Qualifications: 9. First (joint) author publications experience at peer-reviewed AI conferences (e.g., NeurIPS, CVPR, ICML, ICLR, ICCV, and ACL). 10. Direct experience in generative AI and LLM research. 11. Fluent in Python and PyTorch (or equivalent) **Public Compensation:** $177,000/year to $251,000/year + bonus + equity + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.

Description:The Advanced Programs and Exploitation (APEX) team with Lockheed Martin in Boulder is looking for a Research Scientist to support ongoing programs and internal research and development efforts. The APEX team is focused on mission processing applications of remote sensing payloads and fusion of various data types. This position will work alongside research scientists, FPGA engineers, and software engineers on the APEX team to accomplish to develop, test, and deliver prototype and fully capable systems. This position will be expected to: * participate in the development, integration, and enhancement of remote sensing processing and tracking algorithms and software. * evaluate, refine, and develop tracking & processing algorithms. * help our team evolve ground-based mission processing applications of remote sensing payloads onto flight hardware for onboard mission processing operations. * develop a thorough understanding of R&D mission processing code written in C++. * add features to a complex legacy code base. * develop models and detailed simulations to predict and assess system performance. * possibly work on AI/ML algorithm applications. Applicants selected will be subject to a government security investigation and must meet eligibility requirements for access to classified information. This position is in beautiful Boulder, Colorado at our offices which have a collaborative and modern agile workspace. Basic Qualifications: * Degree in a STEM (Science, Technology, Engineering, or Math) field from an accredited institution. * Proficiency in MatLab and another programming language * Ability to obtain a TS/SCI Clearance required for this role. Desired Skills: * Proficient in C++ & Python * Experience with hardware acceleration technologies (e.g., GPUs, FPGAs) * Understanding of AI/ML algorithms and architectures (e.g., CNNs, RNNs, transformers). * Experience in remote sensing * Experience with software version control such as GIT * Applied mathematics or algorithm development experience * Strong experience in software design and development. * Active security clearance Security Clearance Statement: This position requires a government security clearance, you must be a US Citizen for consideration. Clearance Level: TS/SCI Other Important Information You Should Know Expression of Interest: By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings. Ability to Work Remotely: Onsite Full-time: The work associated with this position will be performed onsite at a designated Lockheed Martin facility. Work Schedules: Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits. Schedule for this Position: 9x80 every other Friday off Pay Rate: The annual base salary range for this position in California, Massachusetts, and New York (excluding most major metropolitan areas), Colorado, Hawaii, Illinois, Maryland, Minnesota, New Jersey, Vermont, Washington or Washington DC is $93,200 - $164,450. For states not referenced above, the salary range for this position will reflect the candidate's final work location. Please note that the salary information is a general guideline only. Lockheed Martin considers factors such as (but not limited to) scope and responsibilities of the position, candidate's work experience, education/ training, key skills as well as market and business considerations when extending an offer. Benefits offered: Medical, Dental, Vision, Life Insurance, Short-Term Disability, Long-Term Disability, 401(k) match, Flexible Spending Accounts, EAP, Education Assistance, Parental Leave, Paid time off, and Holidays. (Washington state applicants only) Non-represented full-time employees: accrue at least 10 hours per month of Paid Time Off (PTO) to be used for incidental absences and other reasons; receive at least 90 hours for holidays. Represented full time employees accrue 6.67 hours of Vacation per month; accrue up to 52 hours of sick leave annually; receive at least 96 hours for holidays. PTO, Vacation, sick leave, and holiday hours are prorated based on start date during the calendar year. This position is incentive plan eligible. Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics. The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration. At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work. With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility. If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs, and apply for roles that align with your qualifications. Experience Level: Experienced Professional Business Unit: SPACE Relocation Available: Possible Career Area: Software Engineering Type: Full-Time Shift: First

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Field Research Scientist (Western Kansas, Southern Nebraska, or Eastern Colorado) The Field Research Scientist is responsible for conducting field trials in remote areas that cannot be easily accessed by an established hub. This role supports and manages day-to-day operations of the research program in an assigned territory (Western Kansas), by working with regional Site Leads and key stakeholders to plan, establish, maintain, collect accurate agronomic data from, and harvest corn, soybean, wheat, and winter canola trials. YOUR TASKS AND RESPONSIBILITIES Candidates must be located or willing to relocate in the geographic area of field-testing sites being supported, based near Western Kansas, Southern Nebraska, or Eastern Colorado. The primary responsibilities of this role, Field Research Scientist, are to: * Ensure safe and efficient operation of the research program with respect to budgetary guidelines and expectations. Support the site ESH program as it applies to North American Field Testing and Operations * Selection, preparation and maintenance of multiple field-testing sites. Requires safe driving including frequent trailer use hauling loads in excess of 10,000 lbs; pre-trip inspections and use of logbooks * Plays a vital role is trial preparation including seed processing, packaging, shipping, protocol review, trial placement and mapping/field design; * Maintain field trial sites as weed, insect and disease free; Confident ability in identifying key weeds, insect and disease problems is critical, as is timely and accurate implementation of control measures * With the use of handheld electronic equipment and Monsanto proprietary software, collect notes on various agronomic traits (e.g. emergence uniformity, flowering date, lodging, height, maturity, shattering resistance) in a timely manner throughout the growing season * Harvest plots and collect samples for quality and statistical analysis; ensure harvest data is evaluated and relinquished in accordance with crop advancement deadlines to aid in product advancement decisions * Develop, maintain and implement the use of controlled SOP documents, QMS procedures and investigative protocols * Comply with all regulatory compliance guidelines for Confined Release and Stewarded Trial material; * Collaborate with other Agronomic Research Specialists, Site Leads, and Principal Investigators is expected in order to facilitate efficient trial planning and placement, sharing of ideas and techniques and quick response to issues that may arise (e.g. weather or pests affecting trials); * Works closely with Plant Breeders, Principal Investigators and Agronomic Research Specialists to fully understand the multiple stages of crop development and the importance of each step involved and share experiences cross-functionally as needed; * Field selection, cooperator relations, capable of learning research equipment operations and basic maintenance (all types), field maintenance + data collection, basic agronomic knowledge/crop management, technically savy, adhere to compliance/safety policies, utilization of IT tools, time management, prioritization skills, self-motivated, good decision making abilities. Accountable for business unit or project results through leadership and coordination across site strategy, prioritizing and monitoring projects to ensure completion within deadlines and budgets. Build partnerships and share technical knowledge across sites, involved in industry working groups; * Position entails driving a company vehicle (pooled or assigned to the individual). This may include being required to drive greater than 5,000 business miles annually in a personal, pooled, or rented vehicle OR being expected to frequently drive a pooled car as part of your job duties - regardless of mileage. * Position requires driving for the company that will fall under DOT/FMCSA jurisdiction and will (may) require a CDL. This may entail the hauling of trailers, product, supplies or equipment in a safe manner. WHO YOU ARE Bayer seeks an incumbent who possesses the following: Required Qualifications: * PhD with minimum years relevant experience OR MS with minimum of 2 years relevant experience OR Bachelor's Degree with minimum of 5 years relevant experience; * Valid Driver's License; Driving record (MVR) will be reviewed and must meet guidelines based on the company's Risk Screening for Hiring Drivers; * CDL license or the ability to obtain one within 90 days. Additionally, successful candidate will be placed in a random drug screen pool upon starting the position, per Bayer regulations. (DOT 26k+); * Ability to lift up to 60 lbs.; * Ability to obtain pesticide applicator license; * Ability to obtain UAV license for operating drones; * Ability to work extended hours during peak operational seasons. Preferred Qualifications: * Degree in Agriculture or related field or Agricultural field research experience; * Broad knowledge of crop production and farming practices in corn, soybean, wheat, and/or winter canola; agronomy, plant breeding, and precision agriculture applications; * Operation and maintenance of agricultural research equipment experience; * Effective team leadership qualities including excellent organizational and motivational skills, accurate record keeping and attention to detail; * Strong verbal and written communication skills; * Knowledge of basic statistical analysis and experimental design principles; * Computer skills related to data acquisition and analysis, proficiency in Microsoft Office applications, and precision agriculture technology. Domestic Relocation may be provided for this role #LI-AMSUS Employees can expect to be paid a salary between $75,547.20 - $113,320.80. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 11/03/25. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location:United States : Colorado : Residence Based || United States : Kansas : Residence Based || United States : Nebraska : Residence Based Division:Crop Science Reference Code:855264 Contact Us Email:hrop_*************

Job Description Quantum is now, and it's built here. Oxford Ionics, now part of IonQ, is pioneering the next generation of quantum computing. Using our world-leading trapped-ion technology, we're building the most powerful, accurate and reliable quantum systems to tackle problems that today's supercomputers cannot solve. Joining Oxford Ionics means becoming part of a global IonQ team that is transforming the future of quantum technology - faster, at scale, and with real world impact. What to expect: As a Senior Quantum Scientist, you will be at the forefront of our research and development, taking a leading role in both experimental design and the architecture of future generations of hardware. You will be responsible for driving innovation in coherent control, calibration, and benchmarking at scale, with a particular focus on enabling ultra-low error rates and system reliability across larger trapped-ion devices. Beyond hands-on experiments, you will help shape technical direction, mentor junior scientists, and ensure our work translates into scalable, fault-tolerant systems. What you'll be responsible for: Leading the prototyping and characterisation of advanced coherent control schemes for trapped-ion qubits using laser and microwave fields. Driving system-level benchmarking and optimisation, ensuring near-term devices achieve world-leading performance and stability. Validating and integrating new trap technologies (e.g. on-chip electronics or photonics) to support scaling towards error-corrected architectures. Guiding junior scientists in experimental design, analysis, and presentation of results, while representing Oxford Ionics at external collaborations and conferences. Requirements You will need a PhD in physics or a closely related discipline, with a strong foundation in atomic or qubit-related physics and typically four or more years of post PhD experience in quantum control, either in academia or industry. Alongside deep technical expertise, you should be able to work independently, lead projects, and collaborate effectively within a small, fast-paced team. You will need: Proven expertise in experimental ion-trapping physics, ideally with a focus on quantum information processing and strong programming skills. Hands-on experience in spectroscopy, calibration, benchmarking of qubit systems, and debugging complex experimental setups. Strong proficiency with control software, hardware integration and data analysis. A track record of effective collaboration across teams and clear communication of complex scientific results through publications, talks, or conferences. Benefits Be part of a team that's shaping the future of quantum. We offer more than just a role, you'll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more. Join us and be part of the future of quantum computing. We're proud to be an equal opportunity employer and welcome applicants from all backgrounds. Salary Range $145,000-$175,000 DOE Oxford Ionics is committed to equal opportunity for all.

We are seeking a Senior Advanced Photonics Scientist at our Broomfield, CO or Albuquerque, New Mexico Location. Key Responsibilities: * Participate in a team of physicists and optical engineers supporting the development of commercial and research systems for quantum computing * Design and develop integrated photonic components and systems in novel ways to deliver and manipulate light across the spectrum * Collaborate across disciplines (architecture, physics, photonics, fabrication, mechanical engineering) to define systems and requirements to support quantum computing and demonstrate systems meeting performance requirements * Gather technical requirements, turn them into action plans, and ensure the components and systems meet the requirements * Design novel integrated photonic components to meet challenging specifications * Layout test PICs and work closely with fabrication and test teams to validate photonic component performance * Lead and work with PIC development team and external vendors to ensure timely development and delivery of key demonstrators YOU MUST HAVE: * PhD Degree minimum * Minimum 6+ years of experience (advanced degree inclusive) with photonic integrated circuits (PIC) design using photonic simulation tools (Lumerical, RSoft, or similar guided mode and FDTD solvers) and layout tools (Klayout, GDSFactory, or similar) * Minimum 4+ years' experience (advanced degree inclusive) using and maintaining optical/photonic systems * Due to Contractual requirements, must be a U.S. Person. defined as, U.S. citizen permanent resident or green card holder, workers granted asylum or refugee status * Due to national security requirements imposed by the U.S. Government, candidates for this position must not be a People's Republic of China national or Russian national unless the candidate is also a U.S. citizen. WE VALUE: * PhD Degree minimum (in Optics, Physics, Applied Physics, Electrical Engineering, or a related field) * Experience with design-for-manufacturing * Experience with photonics fabrication processes and metrology * Experience with materials used in visible photonics circuits and optics * Experience in product development regarding photonic design, fabrication and/or packaging of PIC systems * Experience working with cross-disciplinary teams (architecture, physics, fabrication, mechanical engineering, photonics) to develop solutions * Experience leading and mentoring small teams * Broad understanding of optical principles and practices and experience applying this knowledge to projects * Programming experience in Matlab, Python, C * Experience with testing and data analysis (taking, plotting, analyzing, fitting and interpreting relevant data from optical testing experiments) $140,000 - $175,000 a year Compensation & Benefits: Non-Incentive Eligible The pay range for this role is $140,000 - $175,000 annually. Actual compensation within this range may vary based on the candidate's skills, educational background, professional experience, and unique qualifications for the role. Quantinuum is the world's largest integrated quantum company, driving breakthroughs in materials discovery, cybersecurity, and next-generation quantum AI. With a team of more than 600 employees, including more than 420 of them being scientists and engineers, we are leading the worldwide quantum computing revolution. By uniting best-in-class software with high-fidelity hardware, our integrated full-stack approach is accelerating the path to practical quantum computing and scaling its impact across multiple industries. As we celebrate the International Year of Quantum, there has never been a more exciting time to be part of this rapidly evolving field. By joining Quantinuum, you'll be at the forefront of this transformative revolution, shaping the future of quantum computing, pushing the limits of technology, and making the impossible possible. What is in it for you? A competitive salary and innovative, game-changing work Flexible work schedule Employer subsidized health, dental, and vision insurance 401(k) match for student loan repayment benefit Equity, 401k retirement savings plan + 12 Paid holidays and generous vacation + sick time Paid parental leave Employee discounts Quantinuum is an equal opportunity employer. You will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status. Know Your Rights: Workplace discrimination is illegal We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Dive in and do the best work of your career at DigitalOcean. Journey alongside a strong community of top talent who are relentless in their drive to build the simplest scalable cloud. If you have a growth mindset, naturally like to think big and bold, and are energized by the fast-paced environment of a true industry disruptor, you'll find your place here. We value winning together-while learning, having fun, and making a profound difference for the dreamers and builders in the world. We are looking for a Senior User Researcher who is passionate about deeply understanding our customers' needs, context, and motivations. You will accelerate innovation and drive value by bringing these insights to everything we do at DigitalOcean. As a Senior User Researcher at DigitalOcean, you'll join a dynamic team dedicated to revolutionizing cloud computing and AI. Reporting to the Manager of User Research, you will act as a critical link between our users and our business. You'll work with product and design teams to guide the future of our business by generating actionable insights that ensure our products and services meet the everyday needs of our users. You'll lead research for critical customer journeys and products, serving as a strong advocate for applied research and a user-centered mindset across the organization. In addition to leading tactical and strategic studies, you will lead the charge on our continuous research programs that elevate overall "customer intelligence" across the organization. Working with your fellow researchers and strategy leaders, you'll also help shape the team's culture, ways of working, and approach to ResearchOps. What You'll Do: * Lead Targeted Research from End-to-End: Drive end-to-end strategic and tactical research initiatives that both inform and align with high-level business goals and product roadmaps. Manage the full research lifecycle, from planning and recruiting to analysis, synthesis, and final reporting. * Generate Actionable Insights from Disparate Data Sources: Develop and optimize continuous research mechanisms to aggregate and integrate disparate data sources into a cohesive and actionable narrative. Translate complex data into clear insights that drive product decisions and champion the voice of the customer. * Influence, Advocate, and Mentor: Build and maintain strong cross-functional partnerships with product, design, and technical leaders to embed the user perspective. Mentor researchers and coach extended teams to elevate the quality of practice and increase the organization's user-centricity. * Contribute to Our Research Practice: Help advance our research practice by contributing to, refining, and codifying research methods, guidelines, and documentation. Evaluate and integrate new tooling and help manage the centralized research repository to increase the accessibility and impact of all insights. What You'll Add to DigitalOcean: * 5-8 years' experience planning, conducting, and communicating the findings from user research for digital products and services, ideally with a focus on technical users * BS or MS in Interaction Design, HCI, Cognitive Science, Psychology, or equivalent experience * An excellent ability to understand and articulate user needs, as well as to generate and communicate compelling & actionable insights * Demonstrated experience managing large-scale research initiatives and influencing cross-functional teams * Demonstrated expertise in qualitative and quantitative research methods, with an ability to select and combine approaches to deliver actionable insights; additionally, experience in market research is a plus * Proven ability to apply quantitative methods - statistical modeling, behavioural data analysis, experimental design. * Strong understanding of large-scale data pipelines and how to work with data engineering teams. * Proficient skills in SQL, data visualization tools (Tableau, Looker, etc.), and statistical software (R, Python, SPSS, etc.). * An expert understanding of the digital product lifecycle and the ability to collaborate successfully with designers, technical & business teams * Excellent communication and storytelling skills, with the ability to influence leaders as well as peers * Previous experience within the Cloud computing industry is preferred. Compensation Range: * $140,000 - $177,000 * This is a remote role #LI-Remote Why You'll Like Working for DigitalOcean * We innovate with purpose. You'll be a part of a cutting-edge technology company with an upward trajectory, who are proud to simplify cloud and AI so builders can spend more time creating software that changes the world. As a member of the team, you will be a Shark who thinks big, bold, and scrappy, like an owner with a bias for action and a powerful sense of responsibility for customers, products, employees, and decisions. * We prioritize career development. At DO, you'll do the best work of your career. You will work with some of the smartest and most interesting people in the industry. We are a high-performance organization that will always challenge you to think big. Our organizational development team will provide you with resources to ensure you keep growing. We provide employees with reimbursement for relevant conferences, training, and education. All employees have access to LinkedIn Learning's 10,000+ courses to support their continued growth and development. * We care about your well-being. Regardless of your location, we will provide you with a competitive array of benefits to support you from our Employee Assistance Program to Local Employee Meetups to flexible time off policy, to name a few. While the philosophy around our benefits is the same worldwide, specific benefits may vary based on local regulations and preferences. * We reward our employees. The salary range for this position is based on market data, relevant years of experience, and skills. You may qualify for a bonus in addition to base salary; bonus amounts are determined based on company and individual performance. We also provide equity compensation to eligible employees, including equity grants upon hire and the option to participate in our Employee Stock Purchase Program. * DigitalOcean is an equal-opportunity employer. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.

As a Scientist in the Analytical Services team the candidate will be responsible for executing analytical techniques in support of method acquisition, qualification, transfer and validation for the analysis of raw materials, chemical intermediates and final products that supports Active Pharmaceutical Ingredient (API) manufacturing. Essential duties and responsibilities include but are not limited to: Independently initiate, design and execute laboratory scale experiments using analytical instrument platforms such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, Karl Fischer. Train team members to cover all aspects of analytical services job functions according to job level. Guide work activities of analytical research associates Author and review method validation protocols and reports with adherence to ICH guidelines and internal Agilent standard operating procedures (SOPs). Properly record and summarize experiments in notebooks and reports and present research summaries to internal and external customers. Maintain process compliance integrity by adhering to SOPs and current good manufacturing practices (cGMP) as appropriate. Operate laboratory equipment by following operating instructions, troubleshooting instrumentation and method issues, and performing routine preventative maintenance. Interfaces with various departments and serves as internal consultant for analytical services. Qualifications Bachelor's degree (B. S.) or Master's degree (M.S) in chemistry, or related applied sciences field. 8+ years relevant experience and/or training; or equivalent combination of education and experience. 4+ years of demonstrated expertise in method validation, proficiency in analytical platforms such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, and Karl Fischer. Provide mentorship and technical guidance to research associates, serve as a resource for team development Demonstrated experience with performing and guiding analytical method acquisition, qualification, transfer and validation for the analysis of raw materials, chemical intermediates and final products that supports API manufacturing. Demonstrated experience with adhering to regulatory compliance for analytical method validation pertaining to the manufacture of API's. Ability to skillfully operate multiple instrument technologies (e.g. UPLC, GC, GC/MS, HPLC/MS, FTIR, UV/VIS, IC, ICP/MS, flame AA). Demonstrated experience of analytical test methods used in the testing of oligonucleotide API or related molecules is highly desired. Ability to work independently and with interdisciplinary project teams, understand project requirements, and follow project timelines. #LI-DT1 Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least November 10, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $146,640.00 - $229,125.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: R&D

Who we are: We're transforming one of the world's oldest industries with cutting-edge technology and an innovative approach. Backed by top-tier investors and recognized by Time as one of the "best Inventions of 2024" and Fast Company as one of 2024's "Next Big Things in Tech", Electra is scaling rapidly and we're looking for bold, driven individuals to help us reshape the future of iron production. If you're ready to make a real impact in a company that's redefining heavy industry for a cleaner, smarter world, we want to hear from you. What you will do: As a Senior Scientist for the Analytical Chemistry team, you will focus on the challenging analysis of metals in solutions and solids to support our R&D and engineering teams. This position will be responsible for ICP-OES analysis, instrument maintenance and troubleshooting. It is also expected this scientist will lead technicians performing sample digestions and preparations within the Analytical group. Responsibilities include: Perform routine sample analysis in the turnaround time required Maintain and troubleshoot instrumentation and equipment Strong attention to detail Create and oversee analytical chemistry projects to improve data quality and efficiency Clearly communicate results and uncertainty to the rest of the team Develop and validate new methods to meet new analysis needs Draft clear and concise Standard Operating Procedures as needed Evaluate new technologies and methodologies; recommend their adoption when appropriate Mentor other analysts and technicians with more advanced analytical procedures Assist in general laboratory operations such as inventory, clean up, etc. Read, understand, and comply with all workplace health and safety policies, safe work practices, and company policies and procedures Perform other duties as assigned by supervisor What we need you to bring to the team: Demonstrates advanced expertise in analytical chemistry with a bachelor's degree in chemistry or a related field and a minimum of 8 years of industry experience or 6 years with a master's degree or 3 years with a PhD (excluding internships, co-ops, and academic projects) Experienced in ICP-OES analysis, including method development, instrument maintenance, and troubleshooting Skilled in sample digestion techniques such as microwave digestion aqua-regia four acid digestion and borate or peroxide fusions Proficient with a broad range of analytical instrumentation, including XRF XRD C/S O/N, and UV-Vis Capable of independently planning and executing complex projects with minimal oversight Applies in-depth professional knowledge and judgment to evaluate variable factors and resolve complex technical challenges Demonstrates the ability to creatively and effectively solve problems and adapt techniques to deliver high-quality results Frequently mentors and advises others on complex scientific matters and leads internal initiatives without direct people management responsibilities Understands the interrelationships of different scientific disciplines and guides the development of new policies and ideas Comfortable working in a fast-paced, dynamic environment with shifting priorities and deadlines Collaborates effectively with cross-functional teams Communicates clearly both verbally and in writing Proficient in Microsoft Office applications, including Word, Excel, PowerPoint, Outlook, OneDrive, and SharePoint What we want you to bring to the team: Experience with Agilent ICP Expert software, ICP-MS analysis, method development and troubleshooting Creative approach to employing multiple analytical techniques to confirm research questions Safety-first mindset; share potential risks with others before they result in hazardous outcomes Compensation: The anticipated starting pay range for this position is $100,000-$130,000 and may be more or less depending upon skills, experience, and education Benefits For You: 100% paid premiums across all medical, dental, vision, telemedicine, short-term disability, long-term disability, and basic life insurance plans Reasonable use PTO $1,800 in annual employer HSA contributions (health savings account) Benefits For Your Family: 100% paid premiums across all medical, dental, vision, and telemedicine plans 12 weeks of paid parental leave Benefits For Your Future: 401k with up to 5% matching contributions which vest 100% on day one Eligibility for incentive stock options If you need an accommodation during the application or interview process, reach out to us at ************************'re here to help.

Umoja Biopharma is a game-changing biotech start-up with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington, and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting edge drug development. We are committed to the principles of Diversity Equity and Inclusion and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja as a leader in this front. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma - Your Body. Your Hope. Your Cure. POSITION SUMMARY Umoja is seeking a Scientist to join the Downstream Process Sciences team. This position will provide scientific technical leadership for purification of lentiviral vectors through process development, characterization, scale up and technology transfer activities. This position will focus on the optimization and characterization of a lentiviral vector manufacturing process, from experimental design through data analysis and communication. This includes hands-on lab execution and applies Quality by Design (QbD) principles to support the development of multiple clinical products and future transition to a commercial process. A successful candidate should have a thorough understanding of purification techniques including chromatography, tangential flow filtration (TFF) and normal flow (NF)/dead end filtration. This is a fully onsite role based out of our Louisville, CO location. CORE ACCOUNTABILITIES Specific responsibilities include: Perform experimental design, execution, data analysis and communication of results for developing optimized and novel purification operations including nuclease treatment, chromatography, TFF, and normal flow sterilizing filtration for lentiviral vector drug substances and products Collaborate on downstream lab routine operations including adherence to lab safety practices, experiment scheduling, equipment and experiment troubleshooting, solution preparation and detailed documentation in electronic lab notebooks Execute purifications in the lab to support clinical program needs as well as optimization studies, which may include routine purifications to support upstream, drug product, or cross-functional groups. This will utilize small pilot scale equipment (AKTA Avant/Pilot/Ready, Repligen Kr2i, Sartorius Vivaflows and Ambr Crossflow, PendoTech NFF, etc) as well as some in-process analytics (pH, conductivity, particle concentration (ie nanoparticle tracking)) Utilize knowledge of purification fundamentals to not only optimize downstream unit operations, but also inform a process characterization and control strategy for commercial readiness Collaborate closely with the process sciences team (upstream, downstream, drug product, optimization), analytical development (AD), Vector Biology (VB) teams, including mentoring junior employees or contractors and aiding cross-functional experimental design Proactively communicate downstream study progress and risks/mitigations to senior internal and external leaders. Present data, strategies and risks to diverse audiences When needed, serve as downstream subject matter expert on Process/CMC team(s) and support multiple program deliverables Identify opportunities for process and laboratory execution improvements Maintain familiarity with current scientific literature, maintain and update knowledge of current and new purification techniques and instrumentation The successful candidate will have: PhD/MS/BS in Biochemistry, Chemical Engineering, Bioengineering, Biology or related field with 0-2/7/10 years of relevant experience, respectively. Equivalent combination of education and experience will be considered. Extensive expertise in operating lab-scale chromatography systems, TFF systems, and other auxiliary equipment such as balances, pumps, and pH/conductivity meters Extensive experience with experimental design, planning, execution, and basic data analysis Strong team communication and collaboration skills, along with self-motivation to contribute to the development of novel cancer immunotherapies Ability to balance multiple priorities in a fast-paced, cross-functional and dynamic environment Preferred Qualifications: Experience with ÄKTA TM Chromatography systems and UNICORN TM software Experience with TFF and other filtration equipment including the KrosFlo KR2i TM and Ambr Crossflow systems and PendoTech NFF Experience utilizing statistical design of experiment (DOE) to most efficiently execute multi-parameter optimization and design space mapping Experience in clinical phase process development, tech transfer to a manufacturing scale and working in GxP environments Familiarity with Quality-by-Design principles (QbD), small scale model qualification and process characterization for a process control strategy Working knowledge of analytical methods (e.g., nanoparticle tracking (Videodrop), flow cytometry, PCR, ELISA, HPLC) Familiarity with upstream process operations including depth filtration, centrifugation, shake flasks and bioreactors, as well as drug substance and drug product process operations (container closure selection, fill/finish operations) Experience working with electronic lab notebooks Physical Requirements: 100% compliance with personal protective equipment (PPE) requirements in biological laboratory environments for wet lab work, including gloves, protective clothing, and eye safety glasses. Perform physical tasks required for the role, including standing, walking, bending, kneeling, sitting, working your hands in a biosafety cabinet, and occasionally moving materials up to 50 pounds. Project-oriented work in this role will require regular on-site presence to complete essential job-related functions. Salary: $124,440 - $153,720 Benefits Offerings Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

University of Colorado Anschutz Medical Campus Department of Pediatrics | Section of Biostatistics Job Title\: Research Scientist #\:00733832 - Requisition #\:38156 Job Summary: The Department of Pediatrics Section of Biostatistics has an opening for a full-time Biostatistics Research Scientist. This is a key research-faculty position in the Department of Pediatrics for the Biostatistics and Bioinformatics Shared Resource (BBSR) of the University of Colorado Cancer Center. The person in this position will work with investigators on all biostatistical aspects of the research process including the design of new studies, structuring data collection systems, data reduction and analysis, and preparation of abstracts, talks, and manuscripts. In this environment, the BBSR faculty will interact and collaborate with other biostatistics faculty on applied research projects throughout the University. The position will provide biostatistics consulting and collaboration primarily with researchers on cancer-related projects. Key Responsibilities: The Research Instructor position will have four major roles: · (1) to collaborate with Cancer Center researchers on the University of Colorado Anschutz Medical Campus as part of the BBSR; · (2) to collaborate on NIH and other Federal grant submissions; · (3) to provide general consulting in medical data collection and analysis methodology consulting (grants, protocol review, study design, power and sample size, data analysis, abstracts, manuscripts); · (4) to provide education on biostatistics to collaborators and trainees (students, residents, fellows). Work Location: Onsite - this role is expected to work onsite and is located in Aurora, CO. Why Join Us: With an abundance of sunshine and mountains nearby, the Colorado Front Range is the place to be! The University of Colorado Anschutz Medical Campus ranks among the top 20 medical centers in the country. CU Anschutz has top ranked clinical programs in family medicine and pediatrics, and the basic science and applied health research programs attract more NIH funding than any other university in Colorado. CU-Anschutz is home to the University of Colorado Hospital, The Children's Hospital of Colorado, and the University of Colorado Schools of Medicine, Nursing, Dentistry, Pharmacy and Pharmaceutical Sciences, and Public Health, providing access to an array of possibilities to improve lives across a spectrum of ages and disease states. Why work for the University? We have AMAZING benefits and offer exceptional amounts of holiday, vacation and sick leave! The University of Colorado offers an excellent benefits package including: Medical\: Multiple plan options Dental\: Multiple plan options Additional Insurance\: Disability, Life, Vision Retirement 401(a) Plan\: Employer contributes 10% of your gross pay Paid Time Off\: Accruals over the year Vacation Days\: 22/year (maximum accrual 352 hours) Sick Days\: 15/year (unlimited maximum accrual) Holiday Days\: 10/year Tuition Benefit\: Employees have access to this benefit on all CU campuses ECO Pass\: Reduced rate RTD Bus and light rail service There are many additional perks & programs with the CU Advantage. Qualifications: Minimum Qualifications: Applicants must meet minimum qualifications at the time of hire. · Master's degree in biostatistics (received or imminent) · Two years of experience in biostatistical consulting, preferably in an academic setting, or in a hospital, CRO or pharmaceutical setting. Condition of Employment: · Must successfully pass a drug test through Children's Hospital Colorado · Must be willing and able to pass a national criminal background check *For questions regarding Children's Hospital drug testing requirements, please contact Children's Human Resources at ************. Some positions may require testing if access to Children's Hospital or their systems is needed at any time during employment with the University. If drug testing is required, it will be listed in the job posting. Preferred Qualifications: · Demonstrated experience with statistical consulting in a health care field, especially in cancer research. · Excellent R programming skill, experience in RedCap or omic analysis is a plus. · Experience in study design (particularly Phase I/II clinical trials), including sample size and power estimation. · Strong statistical expertise with proficiency in SAS or R for data cleaning, summarization, and advanced statistical analyses (e.g., survival analysis, logistic regression, GLM, longitudinal modeling). Knowledge, Skills and Abilities: · Ability to critically evaluate study aims, identify potential design and analysis pitfalls, and proactively propose solutions to investigators. · Demonstrated ability to manage projects independently, including communicating timelines and setting expectations with collaborators. · Skilled in preparing statistical sections for publications and grant applications. · Competence in data presentation and documentation using tools such as Word, LaTeX, knitr/R Markdown, Excel, PowerPoint, and Adobe. · Excellent oral and written communication skills, with the ability to explain complex statistical concepts to non-statistical audiences. · Experience working effectively both independently and in collaborative team settings. How to Apply: For full consideration, please submit the following document(s): 1. A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position 2. Curriculum vitae / Resume 3. Five professional references including name, address, phone number (mobile number if appropriate), and email address Applications are accepted electronically ONLY at ********************** Questions should be directed to\: ******************************** Screening of Applications Begins: Applications will be accepted until finalists are identified, but preference will be given to complete applications received by 12/1/2025. Those who do not apply by this date may or may not be considered Anticipated Pay Range: The starting salary range (or hiring range) for this position has been established as HIRING RANGE: $80,000 to $100,000 The above salary range (or hiring range) represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. This position is not eligible for overtime compensation unless it is non-exempt. Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans and retirement contributions that add to your bottom line. Total Compensation Calculator\: http\://********************** Equal Opportunity Statement: The University of Colorado (CU) is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities. ADA Statement: The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ****************************** . Background Check Statement: The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees. Vaccination Statement: CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine preventable diseases. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety sensitive job duties, you must enroll in the occupational health medical surveillance program.

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact. Position Summary: The process development (PD) purification Scientist II provides downstream process development input and ownership for a product, including all development and design decisions, with oversight and mentorship from senior process development staff. They can apply scientific principles to design and execute laboratory studies for downstream unit operation development and optimization and solve problems with increasing scope and complexity. They possess a developing working knowledge of the functional area with strong aptitude in one or more downstream (purification) operations (chromatography, TFF, refold, conjugation). They author and review technical documents including protocols and reports commensurate with PD compliance and quality standards. This workflow encompasses process development scope as well as support of technology transfer activities in preparation for cGMP production. Additionally, the PD Scientist II may mentor and train junior staff within the process development group including co-ownership of programs as needed. Technical expertise may be called upon to support troubleshooting or other activities beyond an individual program scope. The PD Scientist II is responsible for maintaining training compliance, according to site expectations. This is a salaried exempt position, with the expectation to cover shift work as needed to support laboratory activities and organizational need. Responsibilities: Downstream (purification) process development, process characterization, and technology transfer of microbial processes to commercial cGMP facility. Works toward developing a broad knowledge of state-of-the-art principles and theory; provides some technical leadership within the group. Responsible for producing high quality documentation and client reports suitable for publication and regulatory requirements. Supports process development in both laboratory and manufacturing settings by executing experiments with guidance, analyzing process data, and contributing to the design and proposal of process development, process improvements, and manufacturing strategies. Will lead the downstream purification portion of development, process characterization, and/or technology transfer programs, acting as subject matter expert, and directing the efforts of the team in meeting the project deliverables. Provide technical support for cGMP manufacturing through floor coverage, batch document review, and support of deviations and change controls with mentor/managerial oversight. Coach and develop departmental scientists. Assist in guiding the professional growth of the team. Responsible for developing/maintaining a current understanding of cGMP and other regulatory requirements. Adheres to all safety requirements and assures that departmental employees comply with required safety procedures. Able to react to change productively and handle other essential tasks as assigned. Chromatography Experience Preferred Requirements: Knowledge, Skills, Abilities: B.S. degree and a minimum of 6+ years of related experience; M.S. and 4+ years of related experience or Ph.D. and 1+ years related experience in a scientific discipline. Language Ability: Records (accurately, clearly, and consistently) information, facts, and measurements that are required by cGMP, GLP, GCP, and/or by co-workers to understand situations and to perform their assignments. Prepares documents using own and others' data; organizes, clarifies, and presents information for internal and external audiences using commonly available software such as MS Office. Reasoning Ability: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions and deal with several abstract and concrete variables. Math Ability: Understands and applies mathematical concepts and methods; interprets data and results using quantitative measures and statistical analysis where necessary; performs and documents calculations and conversions as part of standard processes; develops tests and methods to assure accuracy of processes and measures; learns and applies new quantitative concepts; performs calculations to diagnose or troubleshoot. Computer Skills: Word processing, Spreadsheets, Power Point, E-mail. Equipment Use Computer and lab equipment: Experience with AKTA chromatography skids a plus Salary Range: $101,000 - $138,600 Salary provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be different from the provided value. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid FTO and holidays, 401K matching with 100% vesting upon hire and employee recognition programs. About KBI: KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit ********************* KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds - regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status - and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team. Please note: Our pre-employment drug screening includes substances that are legal in Colorado but remain illegal under federal law, such as marijuana. A positive result for these substances may result in disqualification from employment consideration. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Let's build the future of medicine - together. Join Enveda as a NMR Scientist in Boulder, CO, and help us transform natural compounds into life-changing medicines. We're a team driven by curiosity and innovation - are you ready to make a difference? Boulder, CO | Full-Time | $110,000-$130,000 What Makes Us Enveda Life is smart, and we can learn from it. We're reinventing drug discovery by harnessing nature's intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can't wait. What sets Enveda apart isn't just what we do - it's how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe "People Create All Value", and our success is driven by the extraordinary team turning our mission into reality every day. We're proud of the momentum we've built - * Jan 2024: Named a LinkedIn "Top Startup to Watch" * Mar 2024 & Mar 2025: Forbes America's Best Startup Employers * Oct 2024: First drug to Phase 1 Clinical Trials * August 2025: Raised 150M Series D, gaining Unicorn status These milestones reflect the impact of our team and we're just getting started, but they're only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. Your Role in Our Mission At Enveda, every role drives impact. As a NMR Scientist, you'll be at the forefront of delivering hope to patients everywhere. Your expertise in NMR spectroscopy, instrument maintenance and structure elucidation will be critical in accelerating our mission to advance our pipeline of novel small-molecule therapeutics because every breakthrough starts with bold questions and brave actions. What You'll Do * Design and execute advanced NMR experiments (1D, 2D, and qNMR) to characterize and elucidate the structures of complex natural products. * Automate NMR experiments using IconNMR to maximize instrument efficiency. * Develop and document NMR methods to ensure analytical consistency and data quality. We're Looking For * Ph.D. or M.S. with 1-3 years of experience in relevant fields. * Proven expertise in NMR experimental design and structure elucidation of small molecules. * Experience with high-field NMR instruments, cryoprobes and NMR data processing software. If you're passionate about innovation and impact, we encourage you to apply even if you don't meet every requirement. Our Values: Curiosity | Agency | Journey | Charity | Unity Benefits: 90% Medical, Dental, Vision | 401k Match | Flexible PTO | Adoption Assistance At Enveda, we're building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.

Let's build the future of medicine - together. Join Enveda as a NMR Scientist in Boulder, CO, and help us transform natural compounds into life-changing medicines. We're a team driven by curiosity and innovation - are you ready to make a difference? Boulder, CO | Full-Time | $110,000-$130,000 What Makes Us EnvedaLife is smart, and we can learn from it. We're reinventing drug discovery by harnessing nature's intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can't wait. What sets Enveda apart isn't just what we do - it's how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe “People Create All Value”, and our success is driven by the extraordinary team turning our mission into reality every day. We're proud of the momentum we've built -- Jan 2024: Named a LinkedIn “Top Startup to Watch” - Mar 2024 & Mar 2025: Forbes America's Best Startup Employers - Oct 2024: First drug to Phase 1 Clinical Trials - August 2025: Raised 150M Series D, gaining Unicorn status These milestones reflect the impact of our team and we're just getting started, but they're only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. Your Role in Our MissionAt Enveda, every role drives impact. As a NMR Scientist, you'll be at the forefront of delivering hope to patients everywhere. Your expertise in NMR spectroscopy, instrument maintenance and structure elucidation will be critical in accelerating our mission to advance our pipeline of novel small-molecule therapeutics because every breakthrough starts with bold questions and brave actions.What You'll Do Design and execute advanced NMR experiments (1D, 2D, and qNMR) to characterize and elucidate the structures of complex natural products. Automate NMR experiments using IconNMR to maximize instrument efficiency. Develop and document NMR methods to ensure analytical consistency and data quality. We're Looking For Ph.D. or M.S. with 1-3 years of experience in relevant fields. Proven expertise in NMR experimental design and structure elucidation of small molecules. Experience with high-field NMR instruments, cryoprobes and NMR data processing software. If you're passionate about innovation and impact, we encourage you to apply even if you don't meet every requirement. Our Values: Curiosity | Agency | Journey | Charity | Unity Benefits: 90% Medical, Dental, Vision | 401k Match | Flexible PTO | Adoption Assistance At Enveda, we're building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.

We're Cleerly - a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location. Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks. At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description. While we are mostly a remote company, travel is required for some team meetings and cross function projects typically once per month or once per quarter, for some roles like sales or external facing roles travel could be up to 90% of the time. About the Opportunity We are seeking an accomplished Principal Machine Learning Scientist to lead the development, validation, and deployment of advanced machine learning models that directly impact the diagnostic and prognostic care pathways for heart disease. In this senior-level role, you will provide technical leadership across multidisciplinary teams, help shape the company's ML roadmap, and guide high-stakes projects from ideation through regulatory approval and clinical integration. You will also represent the company in strategic research collaborations with leading academic and clinical institutions, driving innovation at the intersection of AI and cardiovascular health. Responsibilities Lead the design and development of state-of-the-art ML and deep learning models for complex, multi-modal medical imaging and clinical data across multiple projects Define technical and research strategies to achieve new business opportunities, and lead proposals to pursue new areas of science or technology in programs to meet the organization's long-term strategic goals. Set the technical direction for core ML initiatives, balancing scientific rigor with clinical and business priorities. Evangelizes new technology within the company. Drive innovation in data representation, model architecture, and learning paradigms to advance the field and improve clinical outcomes. Establish frameworks and processes that are used across teams. Oversee and guide rigorous validation, benchmarking, and regulatory-aligned evaluation of ML algorithms. Partner with scientific affairs, engineering, product, biostatistician, and regulatory teams to drive the end-to-end lifecycle of medical products to ensure successful delivery and impact. Rally others around a clear vision. Provide support and guidance in all phases of the product development cycle to ensure delivery of high-quality products. Provide design and system optimization solutions to drive improved customer experience and satisfaction. Mentor and guide other ML scientists and engineers, fostering a culture of technical excellence and continuous learning. Lead collaborative research efforts with academic and medical partners; author high-impact publications and contribute to the company's intellectual property portfolio. Present findings, strategic insights, and technical recommendations to executive leadership and external stakeholders. Requirements Ph.D. in Computer Science, Biomedical Engineering, Data Science, or a related technical field. 8+ years of post Ph.D. or industry experience leading applied ML initiatives. Demonstrated technical leadership in developing and deploying ML models in regulated or clinical domains. Recognized expert in machine learning and medical imaging. Deep expertise in machine learning theory and practice, with a strong track record in 3D medical image analysis, including segmentation, reconstruction, registration, restoration, detection, and/or predictive analytics. Strong track record of publications in top-tier machine learning, medical imaging or computer vision Preferred Qualifications 12+ years of post Ph.D. or industry experience leading applied ML initiatives. Hands-on expertise in advanced ML techniques such as vision transformers, self-supervised learning, continual/incremental learning, contrastive learning or physics-informed deep learning. Experience with ML orchestration frameworks, such as Kubeflow, MLFlow, Ray, Metaflow, or Argo Workflow Strong domain knowledge in cardiac CT and coronary artery disease diagnostics. Experience contributing to 510(k) submissions or working in a regulated SaMD development environment. TTC*: CO: $282,000 - $324,000 NY: $288,000 - $348,000 *Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.). Each role at Cleerly has a defined salary range based on market data and company stage. We typically hire at the lower to mid-point of the range, with the top end reserved for internal growth and exceptional performance. Actual pay depends on factors like experience, technical depth, geographic location, and alignment with internal peers. Working at Cleerly takes HEART. Discover our Core Values: H: Humility- be a servant leader E: Excellence- deliver world-changing results A: Accountability- do what you say; expect the same from others R: Remarkable- inspire & innovate with impact T: Teamwork- together we win Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company. OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation. By submitting your application, you agree to receive SMS messages from Cleerly recruiters throughout the interview process. Message frequency may vary. Message and data rates may apply. You can STOP messaging by sending STOP and get more help by sending HELP. For more information see our Privacy Policy (****************************************** All official emails will come *********************** email accounts. #Cleerly

Job DescriptionMosaic Biosciences is a biotherapeutics drug discovery company that partners with biopharmaceutical companies to discover novel protein and antibody therapeutics. Our experienced and dedicated research teams collaborate with our partners to design, manage, and execute research programs to rapidly advance clinical candidates, starting at any point from early discovery into preclinical development. Position Overview: We are hiring a full-time Senior Associate Scientist (I/II) to join our In Vivo Antibody Discovery team. In this role, you will play a critical part in executing hybridoma and/or single B cell screening workflows to identify and characterize antibodies for therapeutic use. You will work under the guidance of scientific leadership to support immunization studies, tissue processing, and high-throughput screening - generating the data that fuel Mosaic partners' discovery campaigns. This is a great opportunity for someone who is detail-oriented, curious, and excited to build something new alongside a close-knit scientific team. Key Responsibilities: Support murine immunization studies including coordinating and scheduling Perform tissue processing and prepare samples for hybridoma fusion and/or single B cell workflows Facilitate execution of screening assays including ELISA, FACS, and plate-based binding formats to identify candidate antibodies Perform mammalian cell culture to support hybridoma expansion, antibody production, and screening activities Maintain detailed records of experiments and support data analysis and presentation Work cross-functionally with protein engineering and characterization teams to ensure smooth data handoff and support campaign timelines Contribute to ongoing workflow optimization through troubleshooting and process improvement Qualifications: B.S. or M.S. in Immunology, Cell Biology, Molecular Biology, or related discipline with 3-6 years of relevant lab experience Hands-on experience with mammalian cell culture Experience working with in vivo antibody discovery methods is strongly preferred Ability to multitask, manage time effectively, and work both independently and collaboratively in a fast-paced environment Strong attention to detail, communication, and organization skills Experience in biotech or CRO settings is strongly preferred Location: This is a full-time, in-person position based in Boulder, CO. Compensation Range: $74,000 - $97,000 (Title and compensation will be determined based on experience and level) Mosaic offers competitive, flexible benefits, including health and dental insurance, disability and life insurance, 401k with company match, and bonus opportunities based on company success. Powered by JazzHR as Tr7Ux6lO

Job Brief: As a Senior Atomic Clock Scientist, you will play a critical role in the development of innovative atomic clock solutions that drive the company's mission forward. The ideal candidate must have demonstrated the ability to set up their own experiments and drive results independently while also collaborating across teams and contributing to product development. Your primary responsibility will be to Design, prototype and test miniaturized optical, mechanical, and electrical systems for chip-scale quantum sensors and atomic clocks. Required Background: PhD or equivalent industry experience in atomic, optical, quantum physics, or 3 years of related academic or industry experience Optical, trapped Ion, or microwave atomic clocks Deep Technical Expertise in the Areas of: Precision spectroscopy Narrow linewidth lasers and laser frequency stabilization Optics, fiber optics, electro/acousto-optics, detectors Analog, digital, and RF electronics Control systems and instrumentation

We are seeking a motivated Associate Scientist to join our Product Sciences team and support the analytical development and characterization of Lentiviral Vector (LVV) and CAR-T cell products. The successful candidate will execute molecular, cellular, biophysical, and biochemical protocols, contribute to routine testing, and maintain high-quality laboratory records. This position works closely with the Senior Scientist and other team members to advance our pipeline and analytical capabilities. Responsibilities * Execute and support bioanalytical assays for characterization of Lentiviral Vector (LVV) and CAR-T cell products, following established protocols and under the guidance of Senior Scientists. * Perform routine and advanced laboratory experiments to assess T-cell binding, activation, transduction efficiency, payload expression, and antigen-specific cytotoxicity. * Prepare and maintain detailed experimental records in electronic lab notebooks, ensuring data integrity and compliance with company standards. * Assist in the development, qualification, and transfer of analytical methods. * Maintain clear and accurate records of experimental work using an electronic notebook system in accordance with company guidelines. * Prepare summaries of technical data and contribute to technical reports. * Support documentation for IND submissions by compiling data, preparing technical reports, and contributing to method write-ups. * Collaborate with cross-functional teams, including Research and Process Development, to coordinate sample testing and share results. * Participate in troubleshooting and optimization of assays as needed, contributing to continuous improvement of analytical workflows. * Adhere to company policies and exemplify core values to ensure safety and quality of gene therapy products and facility. Essential Skills * Experience with in vitro mammalian cell culture and associated wet lab skills. * Proficiency in pipetting, FDA regulations, aseptic techniques, ELISA, PCR, and protein quantifications. * Ability to prepare for IND work and conduct flow cytometry. * Strong organizational skills and attention to detail. * Effective written and verbal communication skills. * Ability to work collaboratively in a multidisciplinary team environment. Additional Skills & Qualifications * BS in Biology, Biochemistry, or related discipline with 4+ years of experience; or an Associate Degree in life sciences or similar with 6+ years of experience. * Hands-on experience with cell culture, primary cell-based cytotoxicity assays, flow cytometry, dd PCR, MSD, JESS, and ELISA. * Excellent communication skills with the ability to build open and collaborative relationships. * Experience with viral vectors, such as LVV, is a plus. * Experience with experimental design, execution, and basic data analysis is a plus. * Self-motivation, organization, effective communication, and presentation skills. * Ability to work in a fast-paced environment, meet deadlines, and prioritize work on multiple projects. Work Environment The team consists of four members, including this position. The role requires 100% compliance with personal protective equipment (PPE) requirements in laboratory environments, including gloves, protective clothing, and eye safety glasses. Physical tasks involve standing, walking, bending, kneeling, sitting, working hands in a biosafety cabinet, and occasionally moving materials up to 50 pounds. The work schedule is Monday to Friday, 9am to 5pm. Pay and Benefits The pay range for this position is $42.91 - $53.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Louisville,CO. Application Deadline This position is anticipated to close on Nov 12, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Company: Dedham Group Employment Type: Full Time **Description** **About The Dedham Group:** We set out to develop a health care innovation organization that could separate the background "noise" from what warrants investment in our highly complex, rapidly evolving marketplace lacking transparency to enable our pharmaceutical and biotech clients to make better decisions and flourish. Today, ten years later, we are the preeminent U.S. market access oncology and specialty strategy partner, grounded in the structure and logic of the strategy consulting discipline, bolstered by our robust data set continuously enriched via our unequaled specialty access panel of the most highly influential access and value influencers in the U.S. With a unique staffing model of highly structured and collaborative creative thinkers akin to an oncology and specialty think tank, we have increasingly come to be viewed as an influencer in our industry. At the interface of clinical, economic, and operational evolving needs, the Dedham Group has become the go-to resource for addressing the challenges faced by the world's leading life sciences organizations. Now, The Dedham Group is proud to be a part of Norstella (*************************** , an organization that consists of market-leading pharmaceutical solutions providers united under one goal: to improve patient access to life-saving therapies. Within this organization, The Dedham Group plays a key role helping commercial teams navigate the oncology space to get much-needed drugs to market-and helping clients connect the dots from pipeline to patient. **About the Consultant role:** As a Consultant, you will works closely within teams and clients to lead primary and secondary research, develop logical and insightful qualitative and quantitative analyses, and create innovative and effective recommendations. **To succeed in this role, you will:** + Contribute to day-to-day management of 3+ projects, guide overall strategic direction and delegation of tasks to team members, parachute where needed across workstreams to streamline execution + Be responsible for timely and successful project execution + Provide direct feedback to junior staff to support career development goals + Support client relationships, fulfill client requests and begin to forecast future project needs + Aid in developing project proposals and capabilities decks to support overall firm development + Communicate clearly with senior project managers on project responsibilities, progress, alignment to timeline, and bandwidth of teams + Other duties as assigned **Requirements** + Bachelor's or advanced degree with a life science focus + 4+ years life sciences Market Access consulting + Superior skills in using MS Office (particularly PowerPoint and Excel) + Excellent oral and written communication skills + Strong collaboration skills; must be a team player + Strong attention to detail + Expert knowledge of provider and payer dynamics within healthcare, specifically within oncology, cellular therapy / CAR-T, immunology, neurology / CNS, and/or other rare diseases / specialty therapeutics **The Guiding Principles For Success At Norstella** **01: Bold, Passionate, Mission-First** We have a lofty mission to Smooth Access to Life Saving Therapies and we will get there by being bold and passionate about the mission and our clients. Our clients and the mission in what we are trying to accomplish must be in the forefront of our minds in everything we do. **02: Integrity, Truth, Reality** We make promises that we can keep, and goals that push us to new heights. Our integrity offers us the opportunity to learn and improve by being honest about what works and what doesn't. By being true to the data and producing realistic metrics, we are able to create plans and resources to achieve our goals. **03: Kindness, Empathy, Grace** We will empathize with everyone's situation, provide positive and constructive feedback with kindness, and accept opportunities for improvement with grace and gratitude. We use this principle across the organization to collaborate and build lines of open communication. **04: Resilience, Mettle, Perseverance** We will persevere - even in difficult and challenging situations. Our ability to recover from missteps and failures in a positive way will help us to be successful in our mission. **05: Humility, Gratitude, Learning** We will be true learners by showing humility and gratitude in our work. We recognize that the smartest person in the room is the one who is always listening, learning, and willing to shift their thinking. **Benefits** + Medical and prescription drug benefits + Health savings accounts or flexible spending accounts + Dental plans and vision benefits + Basic life and AD&D Benefits + 401k retirement plan + Short- and Long-Term Disability + Paid parental leave + Paid time off **_Please note- all candidates must be authorized to work in the United States. We do not provide visa sponsorship or transfers. We are not currently accepting candidates who are on an OPT visa._** _The expected base salary for this position ranges from $150,000 to $175,000. It is not typical for offers to be made at or near the top of the range. Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, licensure or certifications obtained. Market and organizational factors are also considered. In addition to base salary and a competitive benefits package, successful candidates are eligible to receive a discretionary bonus._ _All legitimate roles with Norstella will be posted on Norstella's job board which is located at norstella.com/careers. If a role is not posted on this job board, a candidate should assume the role is not a legitimate role with Norstella. Norstella is not responsible for an application that may be submitted by or through a third-party and candidates should proceed with extreme caution if a third-party approaches them about an open role with Norstella. Norstella will never ask for anything of value or any type of payment during or as part of any recruitment, interview, or pre-hire onboarding process. If you are aware of or have reason to believe a job posting purportedly for a role with Norstella is fraudulent or otherwise not authorized by Norstella, please contact the Company using the following email address:_ _[email protected]_ _._ _The Dedham Group is an equal opportunity employer. All Job applicants will receive equal treatment regardless of race, creed, color, religion, alienage or national origin, ancestry, citizenship status, age, physical or mental disability or handicap, medical condition, sex (including pregnancy and pregnancy-related conditions), marital or domestic partner status, military or veteran status, gender, gender identity or expression, sexual orientation, genetic information, reproductive health decision making, or any other protected characteristic as established by federal, state, or local law._ _Sometimes the best opportunities are hidden by self-doubt. We disqualify ourselves before we have the opportunity to be considered. Regardless of where you came from, how you identify, or the path that led you here- you are welcome. If you read this job description and feel passion and excitement, we're just as excited about you._ Norstella is an equal opportunity employer. All job applicants will receive equal treatment regardless of race, creed, color, religion, alienage or national origin, ancestry, citizenship status, age, physical or mental disability or handicap, medical condition, sex (including pregnancy and pregnancy-related conditions), marital or domestic partner status, military or veteran status, gender, gender identity or expression, sexual orientation, genetic information, reproductive health decision making, or any other protected characteristic as established by federal, state, or local law.

Cascade Bio is seeking an innovative and self-driven Scientist to join our early-stage startup. In this role, you will be responsible for synthesizing and characterizing Cascade's Body Armor for Enzymes™ polymer brush technology. This position offers the opportunity to shape polymer design strategy, scale our technology, and collaborate cross-functionally to drive product performance and scalability. We're looking for a Scientist who embodies our core values: an obsession with delivering top-caliber products to customers, active curiosity, consistent communication, and an inherent assumption of goodwill. The ideal candidate shares Cascade's vision of empowering enzymes to disrupt the chemical industry and is motivated to translate cutting-edge polymer science into impactful, sustainable technology. Responsibilities Develop the design, synthesis, and optimization of Cascade's Body Armor for Enzymes™ polymers using advanced polymerization methods (e.g., controlled radical polymerization). Synthesize new monomers for enhanced stability of immobilized enzymes. Analyze Cascade's Body Armor for Enzymes™ using analytical techniques such as FTIR, Raman, TGA, and other relevant methods. As an early hire at a startup, you must be able to adapt to rapidly evolving project needs and fast paced project timelines. Collaborate across teams to scale our commercial products from lab to commercial scale. Identify and resolve technical challenges in process optimization and reproducibility. Mentor and guide Research Associates on experimental design, data analysis, and best practices. Contribute to project planning, strategy discussions, and technical decision-making. Prepare and present detailed reports, SOPs, and technical summaries to cross-functional teams and leadership. Qualifications Bachelor's degree in Chemistry, Materials Science, or Chemical Engineering with 3-5 + years of startup, industry or research experience in material characterization, polymer chemistry, or related disciplines. Proven track record in polymer synthesis and characterization. Experience with controlled radical polymerization (e.g., ATRP, RAFT) and surface modification techniques is a plus. Strong analytical background in polymer characterization tools (FTIR, Raman, TGA). Experience with process development and scale-up. Prior experience in an early stage startup or fast-paced R&D environment. Proactive approach to troubleshooting experimental issues and proposing innovative solutions. Strong teamwork skills with the ability to collaborate with multidisciplinary teams. Excellent organizational, documentation, and communication skills. Knowledge of laboratory safety protocols and commitment to maintaining a safe working environment About Cascade Biocatalysts At Cascade Biocatalysts, we are commercializing our Body Armor for Enzymes™ technology, an advanced polymer material that enhances enzyme stability and reliability for cost-effective biomanufacturing. Join us in revolutionizing sustainable chemical manufacturing through the power of enzymes and polymers. Your contributions will help create a greener and more sustainable future. Cascade Biocatalysts is an equal opportunity employer. We welcome and encourage diversity in the workplace and strongly encourage candidates from all backgrounds to apply. Salary Range: $80,000-$120,000