Average salary: $170,000 /yearly
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$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...SuggestedFull timePart timeFor contractorsWorldwide$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...SuggestedFull timeLocal area$159.7k - $199.6k
...Associate Director, Regulatory Affairs CMC Join to apply for the Associate Director, Regulatory Affairs CMC role at Acadia Pharmaceuticals Inc. Seniority Level: Director Employment Type: Full-time Job Function: Legal Industries: Pharmaceutical Manufacturing...SuggestedFull timeWork at officeLocal areaRemote workWorldwideNight shift3 days per week$172k - $187k
...Associate Director, CMC Regulatory Affairs Join to apply for the Associate Director, CMC Regulatory Affairs role at Alkermes Regulatory Affairs Chemistry, Manufacturing, and Controls (CMC), plays a critical role in supporting a diverse portfolio of small molecule...SuggestedFull timeWork at officeLocal area- ...A prominent pharmaceutical company is seeking an Associate Director, Regulatory Affairs CMC in San Diego, CA. This leadership role involves developing global regulatory strategies for small molecule therapeutics, coordinating across multidisciplinary teams, and ensuring...SuggestedFull timeWork at office3 days per week
$168k - $356.25k
...Director / Senior Director, Regulatory Affairs (Clinical & CMC) August 2025 Department: Regulatory Position Summary: The Director/Senior Director, Regulatory Affairs will lead and execute global regulatory strategy and operations to enable the development of...SuggestedFull timeTemporary workFlexible hours- ...leading biopharmaceutical company is seeking an Associate Director of Regulatory CMC. This role involves developing global CMC regulatory strategies... ...and at least 8 years of experience in CMC Regulatory Affairs. Excellent organizational skills, attention to detail, and...SuggestedFull time
$302.01k - $390.83k
...Head of CMC Regulatory Affairs Strategy and Operations Join Gilead Sciences to lead the strategy, planning, and execution of CMC Regulatory Affairs for lifechanging therapies. Strategy & Capability Building Develop a roadmap that fosters innovation in CMC RA...SuggestedFull timeLocal area- * Oversee digital modernization of core CMC RA platforms (e.g., RIM) and integration across systems.* Stand up for CMC RA (with enterprise... ...scientific discipline is strongly preferred.* Experience in regulatory operations, strategic planning, and operational execution of...SuggestedFull time
$172.2k - $286.9k
...Chemistry, Manufacturing, and Controls (CMC) & Combination Products (CP) Internal Medicine... ...the development and execution of global regulatory strategies for the assigned drug/device... ...This role involves overseeing regulatory affairs staff, various outside contractors,...SuggestedFor contractorsLocal areaWorldwide$212.5k - $250k
...Hybrid Employee Value Proposition: Join our dynamic and expanding mid-size company in the role of Director for Regulatory CMC directly reporting to Executive Director, Regulatory CMC. Your expertise will play a pivotal and visible role in advancing...SuggestedFor contractorsLocal area$170k - $225k
...strong biological validation. Role Overview The Associate Director, Regulatory Affairs Reporting will be responsible for performing and managing... ...documentation to support project teams Interface with CMC, nonclinical research and clinical research personnel and...SuggestedFull timeRemote workShift work- ...Associate Director of CMC, Quality Assurance (San Diego) job at My Next Stage. San Diego, CA. Working with Us Challenging. Meaningful... ...risks within the Quality organization. Collaborate with Regulatory to track/own Quality input for ongoing regulatory filings and...SuggestedFull timeLive inRemote workShift work
$235k - $260k
...Septerna Director of Regulatory Affairs Septerna is a biotechnology company based in South San Francisco, CA, focused on developing lifechanging... ...coordinate and prepare for regulatory meetings. Partner with CMC, Nonclinical, and Clinical teams to ensure compliance with...SuggestedFull time$220k - $270k
...please go to , and follow us on X or LinkedIn . Reporting to the Chief Technical Officer, we are currently hiring a Director, CMC Regulatory Affairs, to join our Technical Operations team. This position is responsible for leading CMC regulatory activities and...SuggestedFull timeCurrently hiring- ...Title: Associate Director of Regulatory Strategy A rapidly growing pharmaceutical company is expanding its regulatory leadership team and seeking... ...B/C, INTERACT, Scientific Advice), with particular focus on CMC, clinical, and combination product matters. Lead...
$255k - $315k
...Director/Sr. Director Regulatory Affairs Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming,... ...lead, crossfunctional teams (e.g., research, clinical, and CMC teams) Skilled in developing regulatory plans and...Full timeWork at office$300k - $350k
...and more efficiently. About the Position The Senior Director, Regulatory Affairs lead is responsible for developing and directing the regional... ...other relevant regulatory filings. Provides Regulatory CMC guidance around drug development and manufacturing/supply processes...Full timeRelocation- ...Senior Director, Regulatory Affairs Permanent San Francisco, CA Proclinical is seeking a Senior Director, Regulatory Affairs for a growing and... ...providing regulatory guidance to ensure alignment with clinical, CMC, nonclinical, and corporate goals. Oversee preparation,...Permanent employmentFull time
- ...A biopharmaceutical company is looking for a Senior Director of CMC Drug Substance Development & Manufacturing. This role involves leading project oversight for late-stage manufacturing of small molecules and requires a strong background in CMC processes. The ideal candidate...Full time
$240k - $290k
...Director/Sr. Director, CMC Oligo Join to apply for the Director/Sr. Director, CMC Oligo role at GondolaBio GondolaBio is a clinical-stage... ...portfolio, owning all safety/quality, technical, and regulatory deliverables from late lead optimization through IND, clinical...Full timeContract workFlexible hours$240k - $290k
...stage biopharmaceutical company in California is seeking a Director/Sr. Director for CMC Oligo to oversee chemistry, manufacturing, and controls... ...relevant experience, along with demonstrated success in regulatory interactions and CMC leadership in biotech. The role offers...Full timeFlexible hours$255.8k - $401.94k
...leading pharmaceutical company is looking for a Vice President CMC focusing on small molecules and oligonucleotides. The role emphasizes... ...work environment. Candidates should possess over 20 years in regulatory roles, combining leadership and technical expertise. This...Full time- ...Learn more at . The opportunity We are searching for qualified and motivated candidates for the role of Manager Regulatory Affairs (CMC Lifecycle) , based in Sofia. The Manager RA CMC Lifecycle has the responsibility of obtaining and maintaining...Local areaWork from homeWorldwideFlexible hours
- ...commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity The Associate Director of Regulatory Affairs will independently represent regulatory affairs on cross-functional teams and provide targeted, actionable advice...Full timeWork experience placement
- ...Associate Director, Regulatory Affairs Advertising and Promotion Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across crossfunctional teams. RA Ad...Full timePart timeFor contractorsLocal area
$153.6k - $241.34k
...leads global strategies to maximize global regulatory success towards achievement of program... .... Accountabilities The Associate Director will be responsible for complex or highly... ...broad concepts within regulatory affairs and implications across the organization...Minimum wageFull timeTemporary workLocal areaRemote work- ...Associate Director, Regulatory Affairs - Global Labeling Regulatory Affairs Labeling is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams. Regulatory Affairs Labeling creates...Full time
- ...Join to apply for the Associate Director Regulatory Affairs role at BD (Tissuemed Ltd) . We are one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and its no small feat. It takes the imagination and...Full timeRemote work
$175.35k - $219.2k
...About the Job The Associate Director, Regulatory Affairs is responsible for supporting the regulatory function and its activities, the development of regulatory strategy, and contributing the regulatory approval process (including US FDA and other regulatory authorities...Full time













