Average salary: $199,062 /yearly
More statsSearch Results: 178 vacancies
$133.2k - $223.2k
...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: Master’s degree in Regulatory Affairs or related field plus 2 years of related experience...
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$78.12 - $130.21 per hour
...the 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 regulatory team in the development and...
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$138.5k - $186k
...of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA with the following requirements: Bachelor’s degree in a scientific field or foreign academic...
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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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...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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$104.17 per hour
...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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...prominent clinical-stage biotechnology company, is seeking a highly motivated and skilled candidate to join their team as a 2024 COOP CMC Formulation Development. The successful candidate will have the opportunity to work in a dynamic and fast-paced environment as part...
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...product (ATMP) modalities including existing protein-based drugs, monoclonal antibodies, and gene therapy assets. The role has end-to-end CMC product responsibilities from pre-clinical to commercial life cycle process development activities, process platform strategies, and...
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...Massachusetts.
The Position Verve is seeking a Director, Analytical Development to provide leadership within the Analytical Development – CMC function. The individual will lead a team of scientists and associates to develop and implement new and improved analytical methods...
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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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...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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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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...purification, tech transfers)
Oversee internal(in-house) and external vendors (domestic & international CDMOs)
Work cross-functionally with CMC & Manufacturing leaders such as Analytical, Drug Product, QA/QC, Manufacturing, Supply Chain, etc.
Author, review and...
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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. The company was founded by...
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...reach over 10 million patients worldwide. Its time for a career you can be proud of.
Process Development Senior Principal Scientist - CMC Team Lead
**Live**
**What you will do**
Lets do this. Lets change the world. In this vital role you will lead a team of...
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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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Title: Contract - Quality Assurance Specialist, CMC
Location: Cambridge, MA and Acton, MA
Reports to: Supervisor, Quality Assurance
About Vedanta Biosciences:
Vedanta Biosciences is a late-stage biopharmaceutical company developing...
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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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...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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...Associate Director, Global Regulatory Affairs, CMC Authoring
You will author global quality regulatory documents and provide input into development of regulatory CMC strategy for the assigned projects (e.g., iNeST) in different stages of development, including...
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