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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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📑 Meets clinical-stage biopharmaceutical client based in the Bay Area is seeking a highly motivated individual to join their growing regulatory affairs group. The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's r ...

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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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📑 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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📑 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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📑 Our client, an exciting and growing Biotech Company, is seeking a Regulatory Affairs professional at the Senior Director level. This role will lead the North America regulatory strategy and work extremely closely with the C-Suite leaders of the business. They are focused on Autoimmune diseases and are based in New Jersey. This is a hybrid role with ...

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📑 Associate Principal Scientist, Regulatory Chemistry, Manufacturing and Control - Product Lead page is loaded Associate Principal Scientist, Regulatory Chemistry, Manufacturing and Control - Product Lead Apply locations USA - New Jersey - Jersey City PRT - Lisbon - Lisbon USA - Pennsylvania - Plymouth Meeting time type Full time ...

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📑 Role Title: Senior Manager/Associate Director, Regulatory Affairs CMCDepartment: Regulatory AffairsFLSA ExemptCORE VALUES Respect ● Passion ● Teamwork ● Integrity ● Honesty ● Commitment ● CollaborationROLE SUMMARYIn this role you will provide CMC strategy input, authoring, and oversight of CMC-related regulatory items to ensure regulatory complianc ...

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📑 Role Title: Senior Manager/Associate Director, Regulatory Affairs CMCDepartment: Regulatory AffairsFLSA ExemptCORE VALUES Respect ● Passion ● Teamwork ● Integrity ● Honesty ● Commitment ● Collaboration<str ...

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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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📑 CMC Regulatory Technical Writer, Associate Director/Director 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 engineere ...

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📑 Senior Director, Regulatory Affairs (Generalist)Hybrid Role - 3 Days in Menlo Park, CAMeet 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 will be supporting Clinical Regulatory and Regul ...

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📑 Senior Director, Regulatory Affairs CMCHybrid - Philadelphia, PAMeet has partnered with a very well-established pharma with hundreds of approved products. They are looking for a Senior Director of Regulatory CMC (small molecule) to join their team. This position will be working across the compan ...

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📑 Senior Director, Regulatory Affairs (Generalist)Hybrid Role - 3 Days in Menlo Park, CAMeet 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 ...

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📑 Hybrid RoleThe Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health Authority submissions, collaborating across the business and with external partners to develop submission content and strategy.Responsibilitie ...

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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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📑 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 lead ...

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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 lead ...

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📑 Senior Director, Regulatory Affairs CMCHybrid - Philadelphia, PAMeet has partnered with a very well-established pharma with hundreds of approved products. They are looking for a Senior Director of Regulatory CMC (small molecule) to join their team. This position will be working across the company's mid-stage, new development pipeline and will be re ...

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📑 Hybrid RoleThe Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health Authority submissions, collaborating across the business and with external partners to develop submission content and strategy.< ...

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📑 Our client is a clinical stage biopharmaceutical company dedicated to improving patients’ lives. They develop multiple precision medicines targeting hallmark cancer resistance mechanisms.Title: Associate Director, Formulation and Drug DeliveryLocation: South San Francisco, California Salary: $175k - 215kPosition Summary:We are seeking an experience ...

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📑 Associate Director/Director, Regulatory Affairs (Oncology)Remote - East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director or Director of Regulatory Strategy to join their team. This role will be reporting into the VP ...

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📑 Remote - Candidates must be located in the United States - Ideally Southern California The Sr. Director/Director of CMC Regulatory Affairs will be responsible for developing, leading and executing CMC regulatory strategies and activities for the organization, including the preparation and filing of BLA submissions. This position is a hands-on role, ...

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📑 FULLY REMOTE The Associate Regulatory Affairs (CMC) role is an entry level regulatory position that provides varying levels of product support to the regulatory Chemistry, Manufacturing and Controls (CMC) department, across regions and phases of development. Support may include organizing, managing and executing on regulatory ...

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📑 FULLY REMOTE The Associate Regulatory Affairs (CMC) role is an entry level regulatory position that provides varying levels of product support to the regulatory Chemistry, Manufacturing and Controls (CMC) department, across regions and phases of development. Support may include organizing, managing and executing on regulatory CMC project ...

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📑 Position would require the candidate to be a W2 employee of DonatechUS Citizenship/Permanent Resident RequiredFULLY REMOTEThe Associate Regulatory Affairs (CMC) role is an entry level regulatory position that provides varying levels of product support to the regulatory Chemistry, Manufacturing and Controls (CMC) department, ...

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📑 Position would require the candidate to be a W2 employee of DonatechUS Citizenship/Permanent Resident RequiredFULLY REMOTEThe Associate Regulatory Affairs (CMC) role is an entry level regulatory position that provides varying levels of product support to the regulatory Chemistry, Manufactu ...

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📑 Must be able to be on site 3 days per week in the San Francisco Bay Area! Key ResponsibilitiesProvide strategic and operational regulatory guidance for cross-functional teams, including CMC, non-clinical, and clinical, in collaboration with project teams and regulatory colleagues.Contribute to the development of global clinical regulatory plans, pr ...

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📑 Remote - Candidates must be located in the United States - Ideally Southern California The Sr. Director/Director of CMC Regulatory Affairs will be responsible for developing, leading and executing CMC regulatory strategies and activities for the organization, including the preparation and filing of BLA submissi ...

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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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📑 Our client is a clinical stage biopharmaceutical company dedicated to improving patients’ lives. They develop multiple precision medicines targeting hallmark cancer resistance mechanisms.Title: Associate Director, Formulation and Drug DeliveryLocation: South San Francisco, California </p ...

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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We ...

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📑 Exciting opportunity with a global pharmaceutical company dedicated to improving health and quality of life for patients around the world. With a commitment to innovation, quality, and accessibility, they strive to make a meaningful impact in the field of healthcare.Position Overview: This innovative organization is seeking a highly experienced and ...

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📑 Director of CMCLocation: San Francisco, CAWorking situation: HybridLevel: DirectorOur client, a blooming biotechnology company, is looking to expand their R&D capacity to support their growing pipeline including a new class of brain therapies. With a passion for treating neurodegenerative and neuropsychiatric disorders, they are at the forefront of ...

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📑 Exciting opportunity with a global pharmaceutical company dedicated to improving health and quality of life for patients around the world. With a commitment to innovation, quality, and accessibility, they strive to make a meaningful impact in the field of healthcare.Position Overview: This innovative organizati ...

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📑 Who we areREGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with ...

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📑 **Associate Director or Senior Principal Scientist, Gene delivery Analytical Strategy**CAROUSEL_PARAGRAPH* Seattle, Washington; Warren, New Jersey * Drug Dev and Preclinical Studies * R1553275 * Full Time * 02/07/2022 ** Share Job**mail_outlineGet future jobs matching this searchor ** Job Description**At Bristol Myers Squibb, we are inspired b ...

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📑 PMV Pharmaceuticals Inc.Job Description: Executive Director, Head of Regulatory AffairsReports to: Chief Development OfficerLocation: Hybrid (2 days a week in Princeton, NJ office)Position OverviewThe Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the company meets its objecti ...

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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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📑 Who we areTogether, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic ...

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📑 Job Description: Associate Director, Downstream Process DevelopmentLassen Therapeutics is a therapeutic antibody discovery and development company dedicated to the identification of novel medicines for serious unmet medical needs. We are currently looking for an Associate Director to oversee downstream process development and manufacturing of early ...

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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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📑 Senior Director / Vice President, Regulatory Affairs - Obesity and Associated Metabolic DiseasesLocation: Charlotteville, VA or Bay Area, CARivus Pharmaceuticals is searching for a Senior Director / Vice President, Regulatory Affairs to set and lead the regulatory strategy to advance a new class of investigational medicines called controlled metabo ...

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📑 By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.J ...

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📑 Director of Regulatory Affairs San Jose, CA REFDESCRIPTIONThe position is independently responsible for development of global regulatory strategy and representation of Regulatory Affairs on R&D project teams. You will be responsible for managing all Regulatory Affairs activities (nonclinical and clinical) for investigational drug-device com ...

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📑 We are currently partnered with a fast growing pharmaceutical company that is seeking aVP/Senior Director, Regulatory Affairs & Quality Assurance.This is a great opportunity to become part of a company at the forefront of advancing CAR T cellular therapy through innovative platforms engineered to offer superior safety, effectiveness, and accessibil ...

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