Average salary: $170,000 /yearly
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$110k - $160k
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Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs or related field plus 2 years of related...
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...4
Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportunity to explore. This role will provide strategic direction and guidance...
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...and therapies to help people build families, stay healthy, and stand up to the world's oldest enemy: disease.
As the Director, Regulatory Affairs CMC you will be responsible for developing and implementing regulatory strategies for US CMC activities throughout the...
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Takeda Development Center Americas, Inc. is seeking a Manager, Regulatory Affairs
CMC in Cambridge, MA to Develop the Global Regulatory Strategy for products in commercial and development phase; ensure timely submission of new submissions (IND, NDA, BLA, JNDA) to various...
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...boundaries of what is possible in order to bring life-changing therapies to patients worldwide.
Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in...
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...quickly have you in front of a live recruiter.
The Opportunity
Description
We're looking for an Associate Director Regulatory Affairs CMC , working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States .
Leads...
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...Learn more about our work, our culture, and what it's like to be a part of our team:
POSTION SUMMARY
Associate Director, CMC Regulatory Affairs is a hands-on and independent role requiring a strong individual who will provide strategic and operational support to...
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...The 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...
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...Who You Are
The Associate Director, Regulatory Affairs (CMC) works closely with the manufacturing department and individual program teams to ensure CMC compliance and promote overall regulatory success. The Associate Director, Regulatory Affairs (CMC) possesses strong...
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Exec Director Regulatory Affairs/CMC
Allakos Inc. is a dynamic clinical-stage biopharmaceutical company developing first-in-class antibody-based therapeutics to treat allergic and inflammatory diseases.
The Executive Director, CMC Regulatory Affairs is responsible...
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The Associate Director of Regulatory Affairs CMC will be responsible for developing, implementing and advising on global Regulatory CMC strategies for new and late stage programs to secure approval of the manufacturing process and control testing for initial clinical trials...
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...Mammoth BioSciences
OPPORTUNITY
Mammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our... ...regulatory knowledge of US and EU
Interface with CMC, nonclinical research and clinical research personnel and...
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Description
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# Job Description
CMC Regulatory Affairs Manager (Remote)
Contract: Thousand Oaks, California, US
Salary: $55.00 Per Hour
Job Code: 347260
End Date: 2024-05-19
Days Left: 27 days, 3 hours left
Apply...
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...Director, CMC Regulatory Affairs
Direct Hire Fulltime Role
Salary Range: $208,000 - $235,000 per year
Location: Redwood City, CA - Hybrid Role
Job Summary:
The position is responsible for providing CMC regulatory strategies and leading the preparation...
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...Responsibilities:
We are inviting applications for the role of CMC 2 Regulatory affairs. Responsibilities:
Well versed in performing CMC compliance activities including Gap Analysis and assessment for Annex 3 comparative table with reference EU Member States...
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...Define and lead the execution of the global regulatory-CMC strategy from early- to late-phase development and NDA/MAA preparations. Provide... ...ideal candidate would have a strong background in regulatory affairs-CMC with expertise in small molecules/solid oral dosage forms...
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...Description:**
BeiGene is seeking an experienced and energetic regulatory professional to manage, evaluate, and complete regulatory... ...for development of strategies, planning, drafting, and managing CMC-related regulatory submissions and HA interactions to meet the...
...recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Director/Sr. Director, CMC Regulatory Affairs to work for a leading Greater Los Angeles area biotechnology company.
The Director/Sr. Director, CMC...
...Job title: CMC Regulatory Technical Writer II
Location: Bridgewater, NJ, Hybrid
Duration: 1 year
SHIFT SCHEDULE 1st shift... ...functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global locations or contract manufacturing...
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...facilities anchored around deep expertise in immunology and complemented by an expanding set of capabilities.
Associate Director, Global Regulatory Affairs, CMC Authoring (Remote)
You will author global quality regulatory documents and provide input into development of...
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