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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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$138.5k - $186k
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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...
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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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...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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Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory
Affairs CMC Submissions
Management in Lexington, MA to establish global submission activities and timelines in partnership with global and cross-functional stakeholders in Pharmaceutical...
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...team.
Position Summary:
ultra focused - Work together to fearlessly uncover new possibilities
The Vice President of CMC Regulatory Affairs is leading the Ultragenyx's CMC Regulatory Affairs function. Ultragenyx have an exciting portfolio with both marketed, late...
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CMC Regulatory Affairs Manager (Remote)
Contract: Thousand Oaks, California, US
Salary: $55.00 Per Hour
Job Code: 347260
End Date: 2024-06-14
Days Left: 26 days, 3 hours left
Apply...
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...highly skilled team dedicated to bringing the promise of tomorrow to the patients we serve.
Role Summary
The Director of CMC Regulatory Affairs is an experienced Regulatory CMC resource specializing in biotechnology products. Your mission is to drive and perform...
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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 various...
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...CA
Contract Duration: 6-18 months
Rate: Negotiable
Responsibilities:
Excellent employment opportunity for a Regulatory Affairs CMC Associate in the Foster City, CA area. Bay area candidates ONLY
Provide Regulatory CMC support for biologic and small molecule...
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...Job Description
Job Description Our Pharmaceutical client is seeking a Director Regulatory Affairs Chemistry Manufacturing & Controls (CMC) to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug...
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...bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Regulatory Affairs CMC Officer for Cytiva is responsible for leading CMC strategies for internal and partner programs.
This position is part...
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...Director, Regulatory Affairs CMC
Pleasanton, CA, USA Req #355
Tuesday, March 26, 2024
Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their...
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...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 Regulatory Affairs...
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...careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
The Regulatory Affairs CMC Manager II will support the site and customer related regulatory affairs and CMC project activities. Work collaboratively...
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Shift: Monday through Friday 8am - 5pm
Length: 12-24 month contract with a possibility of extension or conversion to full-time
Hybrid schedule: 2-3 days onsite
3 must haves:
BA/BS/MS degree in Pharmacy, Chemistry, Biology, Engineering, or other Life Science discipline...
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...position is 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...
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...Description
Reporting to the Vice President, CMC Regulatory, CARGO is seeking an Associate Director, CMC Regulatory to help progress development of our cell-based gene therapy portfolio.
The successful candidate will have a strong background in regulatory CMC with...
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...disease.
Description:
Reporting to the Sr. Director of Regulatory Affairs and Policy, this role will support and lead activities within... ...within the group and across drug development disciplines such as CMC, Nonclinical, Clinical and Quality. This position will be a...
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...S. strategy, the Associate Manager is responsible for ensuring regulatory compliance with relevant regulations and effectively sending timely... ...P reviews, with Pharmacovigilance to coordinate the DERs, with CMC Regulatory for Drug listings for the drug listing updates....