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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...

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📑 R&D CMC Regulatory Affairs Chemical Products Scientist/Sr. Scientist page is loaded R&D CMC Regulatory Affairs Chemical Products Scientist/Sr. Scientist Apply remote type Hybrid locations JPN - Osaka - Osaka JPN - Tokyo - Chiyoda time type Full time posted on Posted Yesterday job requisition id R286746 J ...

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📑 Senior Director, CMC Development- Small Molecule TherapeuticsLocation: Charlottesville, VA or Bay Area, CARivus Pharmaceuticals is searching for a Senior Director, CMC Development to set and lead a scalable CMC strategy to advance a new class of investigational medicines called controlled metabolic accelerators (CMAs) that have the potential to imp ...

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📑 Senior Director, CMC Development- APILocation: Charlottesville, VA or Bay Area, CARivus Pharmaceuticals is searching for a Senior Director, CMC Development to set and lead a scalable CMC strategy to advance a new class of investigational medicines called controlled metabolic accelerators (CMAs) that have the potential to improve metabolic health fo ...

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📑 Senior Director/Executive Director External Manufacturing - Remote I am execlusively partnered with a dynamic clinical stage ophthalmology pharma dedicated to revolutionizing treatments in small molecule (sterile injectables and bringing them to commercialization. They are committed to delivering high-quality products that enhance patients' lives a ...

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📑 THE COMPANYOur client is a biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases.THE ROLEWe are looking for a dynamic and experienced AD/Director of CMC Technical Writing with expertise in biologics to join there team. The successful candidate will ...

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📑 Senior Advisor/Director, Global Regulatory Affairs, CMC, Biotechnology page is loaded Senior Advisor/Director, Global Regulatory Affairs, CMC, Biotechnology Apply locations US, Indianapolis IN time type Full time posted on Posted 2 Days Ago job requisition id R-61024 At Lilly, we unite caring wit ...

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📑 THE COMPANY89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoPEGylated analog of FGF21. Pegozafermin is being developed ...

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📑 If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Associate Director, Regulatory Affairs CMC Full Time Mgr & Dir - R&D/Ops Malvern, PA, US 10 days ago Requisition ID: 1072 The Associate Director, Regulatory Affairs CMC will le ...

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📑 Disc Medicine is seeking a Director, Regulatory Affairs-CMC to serve as the Regulatory-CMC lead for Disc Medicine’s small molecule program pipeline. This position will have close collaboration with the development teams and visibility to the executive leadership with meaningful opportunities for professional development and career growth.The positi ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...

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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...

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📑 A California-based biopharmaceutical company is looking to add an experienced professional to their CMC Quality Control Department as a Writer / Reviewer. In this role, the CMC Quality Control Writer / Reviewer will be responsible for authoring, drafting. reviewing, and approving the Regulatory QC CMC sections of the company's IND/IMPD and BLA/NDA ...

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📑 My client is a clinical-stage biopharmaceutical company focused on developing innovative therapies for rare diseases. They are currently seeking a skilled regulatory professional to join their growing team as Director/ Sr. Director CMC Regulatory Affairs. This role will involve hands-on development and implementation of regulatory strategies for CM ...

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📑 My client is a clinical-stage biopharmaceutical company focused on developing innovative therapies for rare diseases. They are currently seeking a skilled regulatory professional to join their growing team as Director/ Sr. Director CMC Regulatory Affairs. This role will involve hands-on development and implementation of regulatory strategies for CM ...

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📑 Atlas Search is partnered with a smaller but growing biotech with a focus in the CAR-T Cell Therapy space. The company is looking for an exceptional individual with CAR-T Cellular Therapy experience to serve as the CMC Lead, while leading the CMC product strategy for an innovative CAR T pipeline. Direct GMP-compliant manufacturing operations, inclu ...

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📑 Technical Source is currently in search of a CMC Coordinator for our pharmaceutical manufacturing client in the Birmingham, AL area. The qualified candidate will have experience handling activities related to outbound shipping , inbound shipments, and external shipments from vendors.Responsibilities of the CMC Coordinator include:Coordinate with ve ...

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📑 The Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at [email protected] . Associate Director, Global Regulatory Affairs CMC page is loaded Associate Director, Global Regulatory Affairs CMC Apply locations Copenhagen ti ...

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📑 Atlas Search is partnered with a smaller but growing biotech with a focus in the CAR-T Cell Therapy space. The company is looking for an exceptional individual with CAR-T Cellular Therapy experience to serve as the CMC Lead, while leading the CMC product strategy for an innovative CAR T pipeline. Direct GMP-compliant manufacturing operations, inclu ...

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📑 Reference Number: JO-2402-530393Senior Regulatory Affairs Scientific LeaderRate: NegotiableJob Type: PermanentLocation: United States Exciting opportunity at a fast-growing biotech The team are looking for a regulatory affairs scientific lead that has excellent knowledge and skills in CMC, GMP and regulatory affairs.Resp ...

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📑 Location: Remote, with the Global HQ in Greater Boston, so EST or Central working hours. This role would suit an experienced RA CMC professional who wants to work in a smaller team with less hierarchy and more focus on innovation and strategic leadership, who also wants an opportunity to lead both early and late-stage development projects! We think ...

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📑 All Jobs > Associate Director of CMC Regulatory Affairs Associate Director of CMC Regulatory Affairs Fully Remote • US Remote - WA, NM, SD, KS, TX, IN, SC, NC, PA, NY, or MA applicants only Description JOB TITLE: Associate Director of CMC Regulatory AffairsLOCATION: The role is remote in the USA, but only eligible to residents of the ...

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📑 I'm partnered with an SF Bay Area-based clinical staged biopharmaceutical company focused on the treatment of liver and cardio-metabolic diseases. This position will be reporting to the VP of CMC and will support the drug development and manufacturing activities for phase 3 and commercialization at CDMOs and CTLs for Biologic programs.Responsibilit ...

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📑 I'm partnered with an SF Bay Area-based clinical staged biopharmaceutical company focused on the treatment of liver and cardio-metabolic diseases. This position will be reporting to the VP of CMC and will support the drug development and manufacturing activities for phase 3 and commercialization at CDMOs and CTLs for Biologic programs.Responsibilit ...

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📑 Senior Director, Regulatory Affairs (Generalist)Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and w ...

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📑 Senior Director, Regulatory Affairs (Generalist)Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and w ...

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📑 Senior Director, Regulatory Affairs (Generalist)Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and w ...

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📑 Senior Director, Regulatory Affairs (Generalist)Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and w ...

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📑 CMC Process Development Consultant 2023623Location: Greater Boston, MA (Hybrid)Therapeutic Area: OncologyJob Overview: In this role, the main focus will be on managing CMC processes, coordinating with vendors, overseeing drug substance development, and reviewing various documentation.Primary Job Responsibilities: Manage CDMOs and vendors, ensu ...

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📑 **Senior Principal Scientist or Principal Scientist, Gene Delivery Analytical Strategy**CAROUSEL_PARAGRAPH* Seattle, Washington; Warren, New Jersey * Drug Dev and Preclinical Studies * R1553272 * Full Time * 02/07/2022 ** Share Job**mail_outlineGet future jobs matching this searchor ** Job Description**At Bristol Myers Squibb, we are inspired ...

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📑 Job Title: Associate Director, CMC Quality AssuranceReports To: Director, CMC Quality AssuranceFunctional Area: QualityPosition Location: RemoteExempt/Non-Exempt: ExemptAbout Tourmaline Bio, Inc.We are a nimble, driven and accomplished team of entrepreneurs, physicians, and industry experts with a mission to thoughtfully develop transformative medi ...

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📑 The Director, Manufacturing, is responsible for managing the manufacturing operations and associated logistics of the company’s cell therapy programs, including operation of the internal cGMP manufacturing on-site. This person will work with corporate partners and internal and external stakeholders to develop the CMC manufacturing strategy and mana ...

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