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Regulatory Affairs Specialist III
San Jose, CA within
1 | 2 | 3  Jobs 1 to 10 of 23 matches
Regulatory Affairs Specialist
Natera - San Carlos, CA, USA
POSITION SUMMARY The Regulatory Affairs Specialist will be responsible for the preparation of ... Minimum 3 years experience in the device/diagnostic, biologic and/or pharmaceutica...
Glassdoor - 3 Days ago
Regulatory Affairs Specialist
Idexcel - San jose, CA, USA
Regulatory Affairs Specialist Location: San Jose, CA Duration: 1 year Qualifications: A minimum of ... and three years of related experience, or equivalent combination of related education a...
Lensa - 64 Days ago
Principal Regulatory Affairs Specialist
Cepheid - Sunnyvale, CA, USA
Job Summary The Principal Regulatory Affairs Specialist will support assigned project core teams ... Preferred Requirements Class III PMA products experience Expertise with molecular technol...
Lensa - 63 Days ago
Regulatory Affairs Specialist, Advertising and Promotio...
Varian Medical Systems - Palo Alto, CA, USA
Bachelors degree and 3 years of related experience or Masters Degree with 1 year of related ... In-depth knowledge of FDA regulations and their interpretation relevant to medical device ...
Lensa - 62 Days ago
Senior Regulatory Affairs Specialist - Santa Clara, CA, USA
As a Senior Regulatory Affairs Specialist, your job responsibilities will include, but not be limited to: • Participate in new product design and development project teams as regulatory affairs ....
TheJobNetwork - 5 Days ago
Senior Regulatory Affairs Specialist
Cepheid - Sunnyvale, CA, USA
Collaborate with International Regulatory Affairs and other appropriate key stakeholders to determine the impact of proposed manufacturing, packaging, labeling or design changes on current and .....
Lensa - 63 Days ago
Regulatory Affairs Specialist - Software
Proteus Digital Health - Redwood City, CA, USA
This is a Regulatory Affairs function with significant software engineering interaction and review responsibilities. * Assist with the regulatory submission preparations, document filings and ...
Lensa - 63 Days ago
Director Regulatory Affairs
Buxton Consulting - Hayward, CA, USA
At least 3 years of regulatory affairs with experience associated with global submissions.Must have comprehensive understanding of global regulatory requirements for registration, development and ...
Dice - 42 Days ago
Manager, Post Marketing PV Collaboration & Vendor Manag...
Pharmacyclics - Sunnyvale, CA, USA
... Affairs, etc. to ensure post marketing adverse event procedures are supported and to ensure ... Demonstrating in depth knowledge of drug safety case management, regulations and best...
Pharmacyclics - 4 Days ago
Medical Director, Medical Affairs, NIPT - San Jose, CA, USA
Regulatory, Quality, Assay Development, Marketing and Business Development. As part of the Medical ... Preferably, 1-3 years' experience in pharmaceutical or diagnostics industry. Other...
TheJobNetwork - 16 Days ago
1 | 2 | 3  Jobs 1 to 10 of 23 matches
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