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The Opportunity
Description
We're looking for an Associate Director of Regulatory Affairs , working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States .
Works...
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Flexible hours
...world in which human potential is no longer hindered by the burden of disease.
Description:
Reporting to the Sr. Director of Regulatory Affairs and Policy, this role will support and lead activities within the Regulatory group to advance development of the assets...
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Local area
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...will 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 ....
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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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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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$120k - $160k
...to the best 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...
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Minimum wage
Holiday work
Full time
Temporary work
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...Associate Director, Regulatory Affairs - Boston, MA - Permanent
Proclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position located in Boston, MA.
Primary Responsibilities:
The primary focus of this role is...
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Permanent employment
...medicines to patients through looking at and treating disease in a revolutionary way?
What if you could be the first hire in Regulatory Affairs with the opportunity to build a strategy and your team as we expand our clinical pipeline?
What this position is all about:...
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Shift work
3 days per week
...and procedures, to ensure the rapid and successful development and registration of products while maintaining compliance with all regulatory requirements and commitments. Evaluates proposed regulations and advises on impact of such regulations on the company; may...
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Contract work
Local area
Night shift
...We are seeking an individual who is talented, motivated, and passionate about science to join our Regulatory Strategy team. As Senior Director of Regulatory Affairs, the successful candidate will play an important role in guiding new products into the clinic and setting...
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...the 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...
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Minimum wage
Holiday work
Temporary work
Local area
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Worldwide
...About the Job
The Regulatory Affairs (RA) Director is responsible for the development and implementation of a comprehensive global regulatory strategy that supports the evolution and enhancement of FMIs unparalleled global portfolio of assay products, including companion...
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Work experience placement
...Director, Regulatory Affairs
About the Company
Globally recognized biotechnology company
Industry
Biotechnology
Type
Privately Held
About the Role
The Director, Regulatory Affairs will be responsible for developing global regulatory strategies,...
Suggested
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...
Suggested
...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...
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Remote job
Hourly pay
Holiday work
Worldwide
...Therapeutic Areas : Neuro
Job Overview: The Associate Director/Director will develop and implement global regulatory strategies, serving as the regulatory lead for... ...at least 5 years of experience in Regulatory Affairs within the pharmaceutical, biotechnology, CRO,...
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...Our client is seeking a Sr. Director, Clinical Regulatory Affairs to develop regulatory strategies for both non-clinical and clinical programs and lead interactions with regulatory authorities. Reporting to the SVP, Head of Regulatory Affairs, this role will have significant...
...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,...
Remote job
...Senior Director, Regulatory Affairs
About the Company
International labelling organization based in Los Angeles
Industry
Retail
Type
Privately Held
About the Role
The Senior Director, Regulatory Affairs will be responsible for developing and managing...
Worldwide
The Director of Quality and Regulatory Affairs is responsible for developing and implementing the long range regulatory and compliance strategy by leading... ..., Competent Authority interactions (Q-Subs), and associated regulatory operations and processes.Managing compliance...
Work experience placement
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