Average salary: $190,000 /yearly
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- ...commissioning of Protection & Control systems on high-voltage substations • Conduct hands-on protective relay testing using Omicron CMC 256/356 or Doble F6150 • Test relays including SEL-311L, SEL-387, SEL-487, SEL-421, SEL-351S, GE L90, GE D60, and similar •...SuggestedPermanent employment
- ...Vice President, Commercial CMC About the Company Industry leading open-access biologics technology platform Industry Pharmaceuticals Type Public Company Founded 2015 Employees 10,001+ Categories Pharmaceuticals Manufacturing Medicine...SuggestedContract workFor contractors
$138k - $185k
...About This Role: As a Senior Manager, Regulatory CMC Lead, you will provide regulatory CMC expertise to support assigned projects and products, contribute to global CMC regulatory strategy, and where appropriate, lead regulatory submissions and related strategic activities...SuggestedFull timeTemporary workWork at officeLocal area$185k - $250k
...Associate Director/ Director, CMC Regulatory Affairs Department: 58 - Tech Ops Management Employment Type: Full Time Location: Redwood City, CA Compensation: $185,000 - $250,000 / year Description We are seeking an experienced and strategic Associate...SuggestedFull timeTemporary workSummer holidayFlexible hours$182.07k - $235.62k
...Associate Director, Regulatory Affairs CMC Job Description We are seeking an Associate Director, Regulatory Affairs CMC candidate to sit at our Foster City, CA site. Responsibilities: The CMC Regulatory Affairs Associate Director at Gilead is responsible for...SuggestedLocal area$182.07k - $235.62k
A leading biopharmaceutical company in California seeks an Associate Director in CMC Regulatory Affairs to lead regulatory strategy and ensure compliance in biologics development. The ideal candidate will have over 10 years of experience and proven success in executing...Suggested$182.07k - $235.62k
...Position Associate Director, CMC Regulatory Affairs – Biologics Overview Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes medicines in areas of unmet medical need. We focus on HIV/AIDS, liver diseases...Suggested- A leading biotechnology firm is seeking an Associate Director/Director of CMC Regulatory Affairs to guide regulatory activities for its ECO Synthesis platform. The role demands over 8 years of experience in CMC regulatory affairs, familiarity with regulatory submissions...Suggested
- * Oversee digital modernization of core CMC RA platforms (e.g., RIM) and integration across systems.* Stand up for CMC RA (with enterprise thinking) and oversee a digital/AI fluency and enablement team aligned to strategic priorities.* Create guidelines, systems, and processes...Suggested
- A leading biopharmaceutical company seeks an experienced professional to oversee digital modernization of CMC RA platforms in Foster City, California. The role requires strong experience in regulatory operations, strategic planning, and change leadership, along with a PhD...Suggested
$225k - $260k
...Director - Permanent - San Fransico Own and accelerate CMC strategy for innovative protein therapeutics at the highest level. Proclinical is seeking a Director, CMC Biologics to lead and execute Chemistry, Manufacturing, and Controls (CMC) strategies for protein...SuggestedPermanent employment- ...The individual will be responsible for all aspects of AAV based CMC activities. The Individual will collaborate with QA, Regulatory, SMEs, and CMOs for CMC formulation development, method development, process development, storage/inventory management, logistics etc...SuggestedPermanent employmentWork experience placementWork at office
- California State JobsSuggested
$157.59k - $203.94k
...included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description The CMC Regulatory Affairs Project Manager is responsible for supporting the planning, coordination, and execution of CMC regulatory...SuggestedFull timeFor contractorsWork at officeLocal area- ...The Associate Manager – CMC Regulatory Submissions Compliance supports the management of Clinical Trial Application (CTA) pre-submission review processes within CMC Regulatory Affairs. In this role, you will coordinate and review documentation planned for submission to...SuggestedLocal area
$122.49k
...to apply and join us. Experience and contribute to our unique culture while you develop and expand your career! Assistant Director, CMC Project Management Summary Ionis is seeking an experienced CMC project manager to join our team. This role will report to the...Remote work$100 - $150 per hour
...Title: Regulatory CMC Program Manager Location: Hybrid (Remote with travel as needed) Employment Type: Part-Time / Full-Time Direct Reports: No Hourly Range: $100/hr - $150/hr Company Overview: Founded in 2002, Enterey brings a wide range of consulting...Hourly payFull timePart timeRemote work- ...fast paced company passionate about discovering and developing tomorrow’s most innovative cancer therapies. Abdera is seeking a CMC Project Manager, Contractor who will support and coordinate CMC activities across development programs. Principal Responsibilities...Contract workFor contractorsApprenticeshipLocal area
$125k - $160k
...passionate about discovering and developing tomorrow’s most innovative cancer therapies. Abdera is seeking a Scientist/Sr. Scientist, CMC Radiochemistry to join our growing organization. The ideal candidate will develop radiolabeling processes and perform analytical...Full timeTemporary workApprenticeshipLocal area$7,294 - $10,378 per month
Job Description and Duties Effective July 1, 2025, in accordance with the applicable Memorandum of Understanding, the Personal Leave Program 2025 (PLP 2025) was implemented. PLP 2025 requires each full-time employee in Bargaining Unit 19 and related Excluded, Exempt...Permanent employmentFull timePart time$35.82 - $47.41 per hour
Job Posting Provides quality nursing care to patients, implements specific procedures and programs; coordinates work within the department, as well as with other departments; reports pertinent information to immediate supervisor; responds to inquiries or requests for...Hourly payPart timeLocal areaShift work$157.2k - $256.6k
...As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross...Work at officeLocal areaRemote workWorldwideRelocation package3 days per week$158k - $198k
...harboring mutations in the RAS signaling pathway. The Opportunity: This position is responsible for developing and implementing global CMC regulatory strategies. The role involves coordinating CMC regulatory activities to support the clinical development and eventual...Full timeLocal area$7,294 - $10,378 per month
Job Description and Duties Effective July 1, 2025, in accordance with the applicable Memorandum of Understanding, the Personal Leave Program 2025 (PLP 2025) was implemented. PLP 2025 requires each full-time employee in Bargaining Unit 19 and related Excluded, Exempt...Permanent employmentFull timePart time$6,134 - $7,843 per month
Job Description and Duties Effective July 1, 2025, in accordance with the applicable Memorandum of Understanding, the Personal Leave Program 2025 (PLP 2025) was implemented. PLP 2025 requires each full-time employee in Bargaining Unit 1, 2, 3, 4, 5, 6, 7, 9, 11, 1...Permanent employmentFull timePart time$30.26k - $31.14k
Job Description and Duties Effective July 1, 2025, in accordance with the applicable Memorandum of Understanding, the Personal Leave Program 2025 (PLP 2025) was implemented. PLP 2025 requires each full-time employee in Bargaining Unit 16, and related Excluded, Exempt...Permanent employmentFull timePart time$125k - $160k
...spectrometry and other related techniques such as HPLC and spectroscopy. The ideal candidate will support (radio-)chemistry, biologics and CMC teams to adapt the Abdera platform by analyzing bioconjugates, linkers and precursors, formulations, and other samples as required....Full timeTemporary workApprenticeshipLocal area$3,680.4 - $4,705.8 per month
Job Description and Duties Effective July 1, 2025, in accordance with the applicable Memorandum of Understanding, the Personal Leave Program 2025 (PLP 2025) was implemented. PLP 2025 requires each full-time employee in Bargaining Unit 1, 2, 3, 4, 5, 6, 7, 9, 11, 1...Permanent employmentFull timePart time- ...within the organization. Join us in South San Francisco, CA, to be at the forefront of the future of gene therapy. Senior Consultant, CMC Development and Manufacturing GenEdit is looking for an individual who will provide technical and organizational leadership and...Contract workWork experience placement
$5,748 - $6,968.5 per month
Job Description and Duties Effective July 1, 2025, in accordance with the applicable Memorandum of Understanding, the Personal Leave Program 2025 (PLP 2025) was implemented. PLP 2025 requires each full-time employee in Bargaining Unit 19, and related Excluded, Exempt...Permanent employmentFull timePart timeInternship