Average salary: $177,175 /yearly
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- ...Preferred Qualifications Working knowledge of Pharmaceutical functions including: Clinical Operations Regulatory Affairs CMC / Manufacturing Pharmacovigilance Medical Affairs Commercial Operations Understanding of GxP regulations, ALCOA+, Data Integrity...Suggested
- The role is for a CMC Regulatory Affairs Manager, responsible for day‑to‑day internal regulatory activities across development and marketed projects. Responsibilities Manage multiple projects simultaneously with emphasis on CMC while adapting to changing priorities. Maintain...SuggestedContract work
$200k - $240k
...available. Subscribe to our RSS feeds to receive instant updates as new positions become available. The Director, Technical Operations (CMC) is responsible for providing strategic leadership and oversight of drug product development with a primary focus on oral solid...Suggested$190k - $260k
Codera is seeking a Director, CMC - Formulations in San Diego, California, to oversee CMC strategy and contribute to drug product formulations. The ideal candidate will have a minimum of 5 years in pharmaceutical industry experience, a Bachelor’s or higher in life sciences...Suggested- ZS Associates in South San Francisco is looking for an Associate Consultant in CMC Development & Analytics to support pharmaceutical CMC development and analytics projects. The role involves solving complex challenges in drug development and manufacturing while collaborating...Suggested
$200k - $235k
...disability, contact this employer to ask for an accommodation or an alternative application process. Director, Regulatory Affairs - CMC Full Time Professional Berkeley, CA, US 7 days ago Requisition ID: 1008 Salary Range: $200,000.00 To $235,000.00 Annually Ray Therapeutics...Suggested- Exelixis, Inc. in Alameda, California seeks an Associate Director of Stability Management to lead the stability group within the CMC department. This role manages the stability and reference standard programs for both commercial and clinical products, ensuring compliance...Suggested
- ...is currently expanding its pharmaceutical division. As part of this growth, the organization is seeking a Regulatory Affairs Manager CMC to join their Regulatory team in San Francisco. This is an exciting opportunity to play a hands-on role in regulatory strategy and submissions...Suggested
$209k - $260k
Position Summary Reporting to SVP Technical Operations, the Director Technical (CMC) Project Management will provide technical CMC project management support and leadership across all late‑stage development programs through commercialization and lifecycle management. This...Suggested- ...business. Bring your curiosity for learning, bold ideas, courage and passion to drive life‑changing impact to ZS. Associate Consultant, CMC Development & Analytics ZS is looking to hire a Decision Analytics Associate Consultant in its Supply Chain and Manufacturing...SuggestedWork experience placementLocal areaWork from homeWorldwideFlexible hours
- JobRx, Inc. is seeking an Associate Director or Director of Pharmaceutical Development to lead the manufacture of drug products. This role involves overseeing contract manufacturers and collaborating with cross-functional teams to ensure effective drug development and compliance...SuggestedContract work
$221k - $286k
Overview Senior Director, Regulatory CMC - CAR T Cell Therapy provides global leadership and strategic direction for CMC regulatory activities across early and late-stage development through commercialization of autologous CAR T cell therapy products. This role is accountable...SuggestedFor contractorsRemote workRelocationFlexible hours- Summary/Objective The Cost Accountant is responsible for determining, recording, and reporting unit cost factors, provide management with cost and comparative reports along with analyzing actual manufacturing costs and prepare reports comparing standard to actual costs;...SuggestedPermanent employmentLocal areaMonday to FridayNight shift
- ...South San Francisco, California. The TDL will lead Technical Development Teams in formulating Chemistry, Manufacturing, and Control (CMC) strategies for clinical drug candidates. This role encompasses project management, innovation, and strategic decision-making. An ideal...Suggested
$169.1k - $361.9k
...years of experience in the pharmaceutical industry. This role involves leading the development of chemistry, manufacturing, and control (CMC) strategies for drug candidates, ensuring scientific integrity throughout the process. A generous salary range of $169,100 to $361,90...Suggested- A biopharmaceutical company in Redwood City is seeking an Executive Director of Regulatory Affairs CMC to lead the regulatory strategy for drug products. The ideal candidate will have 15 years of regulatory CMC experience and a successful track record in preparing BLAs....
$105k - $120k
...Executive Assistant, Legal, HR and CMC Boston; San Francisco; Seattle Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101...Work at officeRemote work- The University of California - San Francisco is seeking a Product Compliance Professional to oversee contract manufacturing organizations and ensure compliance with regulatory standards including FDA and EMA. You will lead cross-functional teams, manage project timelines...Contract work
$140k - $150k
Project Manager (CMC / Development Operations) Who Are We? Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co‑inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead...Contract workLocal areaRemote work- Kite Pharma seeks a Senior Director of Regulatory CMC for CAR T Cell Therapy to lead global regulatory activities for CMC. This position requires substantial biopharmaceutical experience and aims for compliance in the development and commercialization of innovative therapies...Flexible hours
- ...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...Contract workFor contractors
- Position: Executive Director, Regulatory Affairs CMC Location: Redwood City, CA Job Id: 270-1156 # of Openings: 1 Allakos Inc. is a dynamic clinical-stage biopharmaceutical company developing first-in-class antibody-based therapeutics to treat allergic and inflammatory...
- Glaukos Corporation is seeking a Sr. Scientist II for their Analytical Technologies team based in San Clemente, California. This role will support drug development through analytical method development and validation, collaborating with CROs and CMOs to ensure data quality...
- Swedish Orphan Biovitrum AB (publ) seeks a Drug Substance Lead to manage synthesis processes for small molecules in San Diego, CA. The candidate should have over 10 years in development and GMP-compliant manufacturing, as well as expertise in synthetic organic chemistry...Flexible hours
$170k - $205k
Neurocentria seeks an Associate Director for CMC Natural Products Development in Walnut Creek, California. This role involves leading the extraction and formulation processes for botanical products, managing GMP relationships, and ensuring readiness for clinical trials....- ...San Francisco is looking for a qualified professional to oversee GMP and GLP quality operations at CMOs. The role involves supporting CMC development, ensuring compliance, and managing quality teams. The ideal candidate should have over 10 years of experience in the...
$285k - $320k
BridgeBio is hiring for a CMC Regulatory Lead in San Francisco, responsible for leading regulatory strategies for drug approvals and submissions. Candidates should have extensive experience in Regulatory Affairs CMC within the biotech or pharmaceutical industry and be adept...Remote job$204k
...management, ensuring compliance with regulatory standards and effective negotiations. Candidates should have over 12 years of experience in CMC and external manufacturing, with a strong understanding of GMP and GxP. The position offers a hybrid work model and a competitive...- A leading biopharmaceutical company is seeking a Drug Substance Lead to oversee the manufacturing process for small molecules. This full-time role requires a minimum of 10 years of experience in drug substance development and manufacturing, and proficiency in synthetic ...Full time
- A leading biopharmaceutical company in South San Francisco seeks a Technical Development Principle Scientist in the Analytical Development Department. The ideal candidate holds a Ph.D. and has solid analytical chemistry knowledge, including HPLC, mass spectrometry, and ...