Average salary: $199,062 /yearly
More statsSearch Results: 198 vacancies
...personally, come join our team.
Position Summary:
ultra impact - Make a difference for those who need it most
The Director, CMC QA will report to the Executive Director of CMC QA and be responsible for maintaining strategic responsibility over QA Operations,...
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...of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Masters degree in Regulatory Affairs or related field plus 2 years of related experience...
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...therapeutics with our best-in-class expression and delivery platform.
Job Description:
We are seeking an exceptional Northeastern Co-op, CMC Pharmaceutical Sciences to join our team. The position will work closely with platform science, discovery, preclinical safety, and...
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...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 development and...
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...boundaries of what is possible in order to bring life-changing therapies to patients worldwide.
Join Takeda as a Director, GRA CMC Pharmaceuticals, Oligonucleotides where you will lead the GRA CMC Pharmaceuticals Oligonucleotide regulatory team in the development...
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...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 various stages of development...
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...Together, we are leading the way towards a healthier and more equitable future.
Position Summary
This role will lead and support the CMC strategies and submission including clinical trials applications, marketing applications, agency briefing packages and response to...
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...Job Description
Job Description Salary:
General Summary
The CMC position will be based in Lexington, MA, and will play a key role in the progression to IND and beyond for Orum’s clinical products. This role requires the candidate to lead the company’s CMC efforts...
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...Summary of Position: The Director Regulatory CMC will be responsible for developing and delivering innovative regulatory CMC strategies for product development and approval. With limited guidance from the EVP Regulatory Affairs & Quality Assurance , the incumbent acts...
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...Consultant Regulatory CMC - Permanent - Boston, MA
Proclinical is seeking a Senior Regulatory Affairs Associate or a Regulatory Affairs Consultant with a strong background in CMC post-approval. This permanent position is located in Boston, MA.
Primary Responsibilities...
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...Job Description
Job Description Senior Director, CMC Lead
Company Overview
Repertoire Immune Medicines is a biotechnology company working to unlock and direct the remarkable power of the human immune system to treat cancer, autoimmune disease and infectious disease...
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...Job Description
Job Description Job Description
The Senior Director of CMC Commercial Assets sits within the Pharmaceutical Operations & Technology team (PO&T) and is responsible for the end-to-end strategy of all commercial assets in all therapeutic areas and...
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...Job Description
Job Description Join Frontier Medicines on an exciting journey as our newest Senior Manager/Associate Director in CMC Development, located at either our Boston or South San Francisco office.
As a crucial member of our team, reporting directly to...
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...Job Description
About This Role
This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsibilities include...
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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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...colleagues in quality and commercial organizations to manage pipeline products and bring current products to industry standards.
Represent CMC and GRA on key governance committees and play a critical role in driving the organization towards innovative approaches for the...
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...a key leadership role for the development of the In Vivo franchise at CRISPR. Reporting to the Senior Director of Regulatory Affairs CMC, you will work closely with cross-functional teams and partners to bring multiple novel therapies to patients. As the Regulatory CMC...
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...remote environments where a variety of strengths and diverse backgrounds are connected.
Reporting directly to the Senior Director CMC of Regulatory Affairs, the (Associate) Director of Regulatory CMC will be responsible for the development of regulatory CMC...
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...Waltham, MA
Position Overview/Department Description
The Genomic Medicine Unit (GMU) Chemistry, Manufacturing and Control (CMC) group at Sanofi is dedicated to the establishment of best-in-class manufacturing platforms to support development of life-changing advanced...
...around specific topic areas through peer-reviewed published research manuscripts by authoring publications.
Collaborate with other CMC staff, clinicians, and scientists on the development of research proposals and manuscripts.
Participate in other ongoing projects of...
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