Regulatory Affairs jobs in Fremont, CA
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DIRECTOR, CLINICAL REGULATORY AFFAIRS
Work with Vice President to devise regulatory strategies to ensure rapid and timely approval of products. Develop global regulatory plans to facilitate the progress of programs in all phases of development. Identify risk mitigatio...
| Company | Cymabay Therapeutics |
|---|---|
| Address | Newark, CA |
| Category | Information Technology |
| Job type | Full-Time |
| Date Posted | a month ago See detail |
Director, Clinical Regulatory Affairs
Cymabay Therapeutics
Newark, CA
Work with Vice President to devise regulatory strategies to ensure rapid and timely approval of products. Develop global regulatory plans to facilitate the progress of programs in all phases of development. Identify risk mitigatio...
a month ago seen See more...
- View all Cymabay Therapeutics jobs - jobs in Newark, CA
Head/ Sr Director of Global Regulatory Affairs
Predicine, Inc
Hayward, CA
Responsible for setting strategy and leading the Predicine Global Regulatory Affairs organization. Organize and oversee the preparation, review, and submission of regulatory documents to regulatory authorities for In vitro diagnos...
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- View all Predicine, Inc jobs - jobs in Hayward, CA
Director or Senior Director, Regulatory Affairs
Veranex, Inc.
San Jose, CA
$165,000 - $263,000 a year
Responsible for managing and prioritizing workload for regulatory staff. Develops and establish strategic regulatory plans and interfaces with project team members, both within the organization and with a diverse range of clients,...
a week ago seen See more...
- View all - jobs in San Jose, CA
Director, Regulatory Affairs, Oncology - Job ID: 1311
Ascendis Pharma
Palo Alto, CA
Medical insurance. Vision insurance. Dental insurance. 401(k). Paid maternity leave. Paid paternity leave. Commuter benefits. Disability insurance. Life Insurance (Basic, Voluntary & AD&D)....
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- View all Ascendis Pharma jobs - jobs in Palo Alto, CA
Staff/Principal Regulatory Affairs Specialist (Operations)
Recor Medical
Palo Alto, CA
Manages post market activities, including but not limited to EU MDR and MEDDEV compliant Clinical Evaluation documents for new products and maintain/update existing company Clinical Evaluation Plans (CEPs), Clinical Evaluation Rep...
2 months ago seen See more...
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Senior Regulatory Affairs Specialist (Robotics & Digital Solutions) - Ethicon, Inc.
Johnson & Johnson
Santa Clara, CA
...
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