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PTC Therapeutics
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South Plainfield, New Jersey
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Job Description Summary: The Associate Director, Regulatory Affairs - CMC will be responsible for leading global regulatory CMC strategy for product development and
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Teva Pharmaceuticals
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West Chester, Pennsylvania
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difference with.
The opportunity
The Sr. Director, Global Regulatory Affairs CMC is ... (Dir, Sr Manager, Manager & Associate III).
The Sr Director, Regulatory Affairs CMC is
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Daiichi Sankyo Inc.
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Basking Ridge, New Jersey
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immune disorders.
Summary
The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small
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Abbott
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Basel,
Switzerland
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)** is looking for a
Associate Director Regulatory Affairs Biosimilars
for its global ... prepare high quality regulatory documentation for complex global regulatory submission worldwide
Lead
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AbbVie
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Madison, New Jersey
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Area and support the Manager, Global Regulatory Lead (GRL), Associate Director, or Director, in the ... application review.
· Support CMC sections of major, complex regulatory submissions, including
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SK Life Science, Inc
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Paramus, New Jersey
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>Assist and support Associate Director in managing Contract Development and Research Organizations (CDMO ... CDMO Project proposals and provide feedback to Associate Director prior to selecting a specific vendor
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Actalent
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Paramus, New Jersey
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Job Description:
Assist and support the Associate Director in managing Contract ... distribution documentation of the investigational product.
Assist and support the management of
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Actalent
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Paramus, New Jersey
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Job Description:
Assist and support the Associate Director in managing Contract ... distribution documentation of the investigational product.
Assist and support the management of
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Actalent
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PARSIPPANY TROY HILLS, New Jersey
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Job Description:
Assist and support the Associate Director in managing Contract ... distribution documentation of the investigational product.
Assist and support the management of
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Bristol Myers Squibb
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Dublin,
Ireland
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** , reporting to the Associate Director, Quality Operations. The person covering this position will provide ... requisite quality support to Global Bristol Myers Squibb (BMS) functional groups such as Global Regulatory
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Bristol Myers Squibb
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Dublin,
Ireland
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** , reporting to the Associate Director, Quality Operations. The person covering this position will provide ... requisite quality support to Global Bristol Myers Squibb (BMS) functional groups such as Global Regulatory
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J&J Family of Companies
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Antwerp,
Belgium
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Associate Director in Solid State Sciences & Characterization - 2406176813W
Description ... ) there is a vacancy for an **Associate Director in Solid State Sciences & Characterization . Within
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Takeda Pharmaceuticals
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Boston, Massachusetts
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implementation of global CMC regulatory strategies during development commercialization and post approval LCM ... Director and Head, CMC Regulatory Affairs, Pharmaceuticals.
**How you will contribute
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Regeneron Pharmaceuticals
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Troy, New York
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The Director of CMC Industry and Regulatory Intelligence is responsible for enabling chemistry ... for all CMC operations across Regeneron.
As a Director of CMC Industry and Regulatory
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Bristol Myers Squibb
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Uxbridge,
United Kingdom
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global regulatory CMC strategies and partners with key stakeholders to execute the strategies in ... **
The CMC Regulatory Director, Cell Therapy is responsible for content development, compilation
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Bristol Myers Squibb
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Denham,
United Kingdom
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global regulatory CMC strategies and partners with key stakeholders to execute the strategies in ... **
The CMC Regulatory Director, Cell Therapy is responsible for content development, compilation
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J&J Family of Companies
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England,
United Kingdom
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Senior Manager, Regulatory Affairs, CMC - 2407021125W
Description
Senior Manager, Regulatory Affairs, CMC
Located: High Wycombe, UK (Hybrid)
Who we are
At Kenvue, we
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Takeda Pharmaceuticals
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Boston, Massachusetts
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Director and Head, CMC Regulatory Affairs – Pharmaceuticals.
**How you will contribute ... implementation of global CMC regulatory strategies during development ,commercialization and post approval LCM
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Boehringer Ingelheim
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Ridgefield, Connecticut
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Description
The Associate Director of Drug Substance - EACD will have the primary ... substance technical lead on CMC teams and coordinate activities with regulatory, drug product, analytical
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Teva Pharmaceuticals
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West Chester, Pennsylvania
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Associate Director, Regulatory Affairs - Remote OR West Chester, PA
Date: May 15, 2024 ... difference with.
How you’ll spend your day
As the Associate Director, Regulatory Affairs
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Ascendis Pharma
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Palo Alto, California
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for supporting and developing global regulatory strategies for both development and commercial ... Senior Director, Regulatory Affairs.
Key Responsibilities
Responsible for
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Sanofi Group
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Cambridge, Massachusetts
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the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs, Regulatory CMC ... Our Team:
The Global Regulatory Affairs Device team is a globally diverse team
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Sanofi Group
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Swiftwater, Pennsylvania
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the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs, Regulatory CMC ... Our Team:
The Global Regulatory Affairs Device team is a globally diverse team
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Sanofi Group
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Bridgewater, New Jersey
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the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs, Regulatory CMC ... Our Team:
The Global Regulatory Affairs Device team is a globally diverse team
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Daiichi Sankyo Inc.
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Basking Ridge, New Jersey
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relevant CMC sections of regulatory submissions (INDs/IMPDs, NDAs, BLAs, etc.), responses to regulatory ... “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on
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Daiichi Sankyo Inc.
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United States
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immune disorders.
Summary
Responsible for leading and developing global regulatory ... regulatory strategy is endorsed by GPT and other governance bodies.
Serve as a leader of the GRT (Global
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Daiichi Sankyo Inc.
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Basking Ridge, New Jersey
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immune disorders.
Summary
Responsible for leading and developing global regulatory ... regulatory strategy is endorsed by GPT and other governance bodies.
Serve as a leader of the GRT (Global
...
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J&J Family of Companies
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England,
United Kingdom
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Senior Director, Global Regulatory Leader, CAR-T Therapy - 2406186120W
Description
Johnson & Johnson is currently seeking a Senior Director, Global Regulatory Leader for transformational
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J&J Family of Companies
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Titusville, New Jersey
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Senior Director, Global Regulatory Leader, CAR-T Therapy - 2406186120W
Description
Johnson & Johnson is currently seeking a Senior Director, Global Regulatory Leader for transformational
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J&J Family of Companies
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Raritan, New Jersey
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Senior Director, Global Regulatory Leader, CAR-T Therapy - 2406186120W
Description
Johnson & Johnson is currently seeking a Senior Director, Global Regulatory Leader for transformational
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