| Job alert | Jobs 31 - 40 of 268 |
Medical Device Software Quality Engineer
Kforce
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San Diego, CA
... This is an FDA Medical Quality Engineering position REQUIREMENTS: * BS degree in Engineering, Biotechnology, or Computer Sciences or related field or equivalent combination of education and years of applicable experience * At least 2-5 plus years of ... - May 24
IVD Validation Manager
Genalyte
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San Diego, CA
... WHAT YOU'LL DO Organize and coordinate execution of multiple concurrent verification and validation studies, per the approved protocols, for submission to the FDA for 510(k) clearance. Build a validation team capable of executing studies across ... - Jun 12
Senior Analyst-Programmer I
Wapt
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San Diego, CA
... therapeutic area Advanced knowledge in industry standards, such as the ICH guidelines, CDISC standards, 21 CFR Part 11, and FDA guidelines Demonstrated expertise in the handling and processing of upstream data, e.g., multiple data forms, workflow, ... - Jun 18
Senior Clinical Project Manager
EPM Scientific
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San Diego, CA
... Thorough understanding of clinical trial processes, Good Clinical Practice (GCP) guidelines, and regulatory requirements governing clinical research (e.g., FDA regulations, ICH guidelines). Strong project management skills with the ability to ... - Jun 02
Sr. Regulatory Strategy Manager
Neurocrine Biosciences
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San Diego, CA
... The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple therapeutic areas. For three decades, we have applied our ... - Jun 22
Software Verification & Validation Engineer 1
Hologic
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San Diego, CA
... Perform Verification and Validation testing in an FDA/UL regulated environment. Assist with all aspects of medical device life cycle process, IEC 62304. Troubleshoot product problems, improvements or field complaints. Review data and recommend ... - Jun 07
Associate Director, Clinical Supply
Avidity Biosciences
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San Diego, CA, 92101
... A strong knowledge of cGMP supply, experience working with IRT, manufacturing and distribution operations, and knowledge of cGMP and FDA/EMA guidelines is required. This position will work cross-functionally with clinical development, legal, finance ... - Jun 19
Senior Manager Clinical Operations
Autobahn Therapeutics, Inc.
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San Diego, CA
... Key Responsibilities Responsible for providing sponsor oversight of clinical study conduct (start-up through database lock and reporting) in compliance with Autobahn SOPs, HREC/FDA/EMA/ and other RA regulations, ICH/GCP guidelines and applicable ... - Jun 18
Chemical Support Specialist
Mentor Technical Group
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San Diego, CA
Job Description Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and ... - Jun 22
Director, Clinical Supply
Avidity Biosciences
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San Diego, CA, 92101
... A strong knowledge of cGMP supply, working knowledge of cGCP, experience working with IRT, manufacturing and distribution operations, and knowledge of cGMP and FDA/EMA guidelines is required. This position will work cross-functionally with clinical ... - Jun 19