Regulatory Affairs Medical Device Jobs in Pasadena, California | ComplianceCrossing.com
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Regulatory Affairs Medical Device Jobs in Pasadena






Job info
 
Location
San Fernando, CA
Posted Date
Aug 23, 17
Info Source
Recruiter  - Full-Time   

5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and foreign..

 
Location
San Fernando, CA
Posted Date
Aug 23, 17
Info Source
Recruiter  - Full-Time   

... 5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and..

 
Location
San Fernando, CA
Posted Date
Aug 23, 17
Info Source
Recruiter  - Full-Time   

5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and foreign..

 
Location
San Fernando, CA
Posted Date
Aug 24, 17
Info Source
Recruiter  - Full-Time   

5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and foreign..

 
Location
San Fernando, CA
Posted Date
Aug 24, 17
Info Source
Recruiter  - Full-Time   

5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and foreign..

 
Location
San Fernando, CA
Posted Date
Aug 24, 17
Info Source
Recruiter  - Full-Time   

5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and foreign..

 
Location
San Fernando, CA
Posted Date
Sep 02, 17
Info Source
Recruiter  - Full-Time   

5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and foreign..

 
Location
San Fernando, CA
Posted Date
Sep 02, 17
Info Source
Recruiter  - Full-Time   

... 5-7 years of Class II device experience. MUST have global experience ... review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) ... to the FDA and..

 
Company
Keck Graduate Institute
Location
Claremont, CA
Posted Date
Aug 16,2017
Info Source

Clinical research, regulatory affairs, or quality assurance. Online Form - HR Application - Professor of Practice in Clinical and Regulatory Affairs......

 
Company
Black Diamond Networks
Location
,
Posted Date
Sep 21,2017
Info Source

Provides microbiology support to the Regulatory Affairs department in preparing submissions to regulatory agencies and notified bodies......

 
Company
Black Diamond Networks
Location
,
Posted Date
Sep 21,2017
Info Source

Medical device (specifically IVD) experience. 10+ years ... IVD) experience. 10+ years of Regulatory Affairs experience. Looking for a Regulatory expertise to answer questions in .....

 
Company
DiaSorin
Location
,
Posted Date
Sep 01,2017
Info Source

Requires knowledge of scientific, medical and regulatory terms. Three to five years ... to five years of pre-market regulatory experience in the medical device industry or.....

 
Company
Conceptual MindWorks, Inc.
Location
,
Posted Date
Aug 31,2017
Info Source

Provide subject matter expertise in regulatory affairs supporting MCM development pathways. Clinical and/or regulatory policy;.....

 
Company
Conceptual MindWorks, Inc.
Location
,
Posted Date
Aug 31,2017
Info Source

Provide subject matter expertise in regulatory affairs supporting MCM development pathways. Clinical and/or regulatory policy;.....

 
Job title
Company
Volt Workforce Solutions
Location
Los Angeles, CA
Posted Date
Jul 07,2017
Info Source

Understand and comply to medical device regulatory requirements related to labeling. Must ... Must have current or recent medical device or pharma industry......

 
Company
Pacira Pharmaceuticals
Location
,
Posted Date
Sep 08,2017
Info Source

Minimum two years of relevant experience in pharmaceutical, biological product, or medical device Regulatory;.....

 
Company
Excellent high growth medical company via The Walstrom Group
Location
Los Angeles, CA
Posted Date
Aug 31,2017
Info Source

Minimum 4-5 years experience in regulatory affairs within the Medical Device Industry. Regulatory Affairs Specialist is involved with developing ... Specialist is involved with developing regulatory.....

 
Company
Hydrogen Group
Location
,
Posted Date
Aug 01,2017
Info Source

Must have 5+ years of experience in the medical device industry including but not limited to regulatory reviews and submissions, clinical studies, and.....

 
Company
Fairway Consulting Group
Location
,
Posted Date
Jul 28,2017
Info Source

At least 5 years of clinical trial or medical affairs experience in the pharmaceutical industry or equivalent......

 
Company
Fairway Consulting Group
Location
,
Posted Date
Aug 11,2017
Info Source

Represents the company and Medical Affairs during exchanges with the medical/scientific community. Previous medical device/pharmaceutical industry experience.....

 
Company
TRS Staffing Solutions
Location
Glendora, CA
Posted Date
Sep 18,2017
Info Source

Our client is seeking a Regulatory Affairs /Quality Assurance Specialist to join their team of professionals. In Business or a related technical field preferred.....

 
Job title
GRANTED JOB
Company
STAAR Surgical
Location
Monrovia, CA
Posted Date
Sep 09,2017
Info Source

Minimum of 5 years of hands-on experience in Regulatory Affairs in the medical device or pharmaceutical industry required......

 
Job title
GRANTED JOB
Company
STAAR Surgical
Location
Monrovia, CA
Posted Date
Sep 09,2017
Info Source

Strong working knowledge of medical devices regulations and terminologies. Maintain/Index/Organize Regulatory library......

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