Get new jobs by email
- *No Visas *Must be US Citizen We are seeking a Regulatory Affairs Specialist with a strong background in oral solid dose pharmaceuticals... ...direct experience authoring regulatory submissions, working with API and CMC change management, and have familiarity with scale-up...Suggested
Planet Pharma
Bristol, TN3 days ago - ...API Integration Specialist Nationwide IT Services, NIS, is seeking an API Integration Specialist for the following potential opportunity: Design, develop, and maintain RESTful APIs and integration services using Java, Spring Boot, and microservices patterns. Implement...SuggestedContract work
$153.6k - $241.34k
...Associate Director, Global Regulatory Affairs GI & Inflammation Apply for the role at TakedaPharmaceutical Nordics AB. Job Description Associate Director responsible for regulatory affairs for GI & Inflammation programs. Provides strategic and tactical advice...SuggestedFull timeRemote workTakedaPharmaceutical Nordics AB
Boston, MA5 days ago$170k - $220k
...Overview The Associate Director of CMC Regulatory Affairs will be responsible for creating CMC regulatory development plans and for successful execution against those plans. The Associate Director of CMC Regulatory Affairs represents the function on departmental and...SuggestedFull timeWork at officeLocal areaNight shiftWeekend workAfternoon shift3 days per weekXeris Pharmaceuticals
Chicago, IL5 days ago- ...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
Acadia Pharmaceuticals Inc.
San Diego, CA5 days ago $159.7k - $199.6k
...week on average. Position Summary The Associate Director, Regulatory CMC, is responsible for contributing to/assisting with the... ...activities. Primary Responsibilities Supports CMC regulatory affairs activities for marketed products and compounds in development...SuggestedFull timeWork at officeLocal areaRemote workWorldwideNight shift3 days per weekAcadia Pharmaceuticals Inc.
San Diego, CA5 days ago- ...Senior Regulatory Consultant- Lead - Mexico Responsibilities: Creation of regulatory strategies... ...teams for collating labels and COAs of API, excipients and finished product.... ...experience with minimum 5+ years in regulatory affairs Individuals must have fluency of...SuggestedHourly payPermanent employmentFull timeTemporary workWork experience placementFor subcontractorLocal areaRelocationVisa sponsorship
ClinChoice Inc.
Santa Fe, NM5 days ago $153.6k - $241.34k
...Associate Director, Global Regulatory Affairs, Advertising and Promotion Join Takeda as an Associate Director, Global Regulatory Affairs, Advertising and Promotion . This role involves managing programs/products as the internal expert on US and international codes...SuggestedFull timeRemote workWorldwideTakeda
Boston, MA5 days ago- ...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...SuggestedFull time
Gilead Sciences, Inc.
Foster, CA5 days ago $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 areaGilead Sciences, Inc.
Foster, CA5 days ago$170k - $200k
...A next-generation precision medicine company is seeking an Associate Director of Regulatory Affairs in San Diego, CA. This role develops and implements regulatory strategy while leading cross-functional teams in clinical trials. Candidates should have over 8 years of...SuggestedFull timeMirador Therapeutics
San Diego, CA5 days ago- ...biopharmaceutical company is seeking an Associate Director of Regulatory CMC. This role involves developing global CMC regulatory strategies... ...science and at least 8 years of experience in CMC Regulatory Affairs. Excellent organizational skills, attention to detail, and the...SuggestedFull time
Acadia Pharmaceuticals Inc.
San Diego, CA5 days ago $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 hoursCodexis, Inc.
Redwood City, CA5 days ago- ...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...SuggestedFull timePart timeFor contractorsLocal area
Gilead Sciences, Inc.
Foster, CA5 days ago $153.6k - $241.34k
...Associate Director, Global Regulatory Affairs - GI & Inflammation Join to apply for the Associate Director, Global Regulatory Affairs - GI & Inflammation role at BioSpace. Objective / Purpose Defines, develops and leads global strategies to maximize global regulatory...SuggestedFull timeTemporary workLocal areaBioSpace
Boston, MA5 days ago$190k - $205k
...Associate Director, Regulatory Affairs CMC Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic...Full timeTemporary workWork at officeFlexible hoursShift workOlema Oncology
Boston, MA5 days ago- ...Position Summary We are seeking an experienced and motivated Senior Manager / Associate Director, CMC Regulatory Affairs to support global regulatory strategy and execution for clinical and commercial programs. This role will be responsible for leading CMC regulatory...
Vivid Resourcing
Boston, MA4 days ago $190k - $205k
...A leading biopharmaceutical company is seeking an Associate Director for Regulatory Affairs CMC, based in San Francisco. You will develop and execute regulatory strategies for product development and ensure compliance with global regulations. Ideal candidates have over...Full timeOlema Oncology
San Francisco, CA5 days ago- ...A pioneering healthcare company in Boston is seeking a Regulatory Affairs professional to develop and implement regulatory strategies for innovative cancer detection products. The ideal candidate will have extensive experience in regulatory submissions, particularly with...Full timeFlexible hours
GRAIL
Boston, MA5 days ago $164k - $205k
...An innovative healthcare company based in Washington, D.C., is seeking a Regulatory Affairs professional with at least 10 years of experience to assist in developing regulatory strategies and submissions. This role involves preparing investigational device exemptions...Full timeGRAIL
Washington DC5 days ago- ...Title: Associate Director of Regulatory Strategy A rapidly growing pharmaceutical company is expanding its regulatory leadership team and seeking a strategic, execution-oriented Associate Director of Regulatory Strategy . This role will lead regulatory strategy for...
EPM Scientific
Boston, MA1 day ago $182.07k - $235.62k
...Associate Director, Regulatory Affairs - Virology At Gilead, were creating a healthier world for all people. For more than 35 years, weve tackled diseases such as HIV, viral hepatitis, COVID19 and cancer working relentlessly to develop therapies that help improve lives...Full timeFor contractorsLocal areaGilead Sciences, Inc.
Foster, CA5 days ago$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...Full timePart timeFor contractorsWorldwideGilead Sciences, Inc.
Foster, CA5 days ago$170k - $200k
...Associate Director, Regulatory Affairs - San Diego, CA Mirador is a next-generation precision medicine company focused on immunology and inflammation. The companys Mirador360 precision development engine leverages the latest advances in human genetics and cuttingedge...Full timeBioSpace
San Diego, CA5 days ago$160k - $275k
...Associate Director or Director, Regulatory Affairs Kymera is a clinicalstage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve...Full timeKymera Therapeutics
Boston, MA5 days ago- ...Regulatory Affair Manager Location: San Rafael, CA Duration: 6 Months The Global Regulatory Affairs (GRA) is responsible for obtaining approval for new products and ensuring that approval is maintained throughout the product lifecycle. GRA serves as the interface...
Staffing the Universe
San Rafael, CA2 days ago - ...divh2Job Title/h2pResponsibilities: Regulatory submissions including original ANDAs, amendments, annual reports, supplements and PADERs... ...amendments/supplements as assigned by the director, regulatory affairs or VP, regulatory affairs. Participate in project calls with...
Katalyst Healthcares Life Sciences
San Jose, CA4 days ago - ...Director of Regulatory Affairs (San Francisco, CA) Summary: This role provides global regulatory leadership and expertise to ensure compliance and successful submission of clinical regulatory filings. The position involves developing regulatory strategies, managing...Full time
Cedent
San Francisco, CA5 days ago $197k - $240k
...Associate Director, Regulatory Affairs Join Maze Therapeutics as an Associate Director, Regulatory Affairs, where you will play a critical role in advancing our clinical-stage programs by providing regulatory expertise and executional leadership. As a key member of...Maze Therapeutics
South San Francisco, CA1 day ago$164k - $205k
...information, please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership... .../or global health authorities. Support the U.S. Regulatory Affairs team in preparing submissions such as PMAs, 510(k)s, post-approval...Full timeLocal areaFlexible hoursGRAIL
Washington DC5 days ago
