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Resume alert |
Resumes 1 - 10 of 316 |
San Diego, CA
... pulse generator devices • Identified root cause and troubleshoot defective electroporation medical devices • Complied with the FDA policies, guidelines and regulatory requirements • Performed and documented all activities in compliance with Good ...
- May 02
La Jolla, CA
... Applied continuous pressure to quality assurance FDA mandates, currently to two non-conforming production lot receipts and from additional past remediation effort issue discretions which resulted in the supplier issuing our company $111,000+ in a ...
- Apr 29
National City, CA
... - Adhere to the FDA rules and regulations. - Inspect parts for dents, damage, and missing components. - Perform area clearance before and after each shift. - Participate in group training with leads and supervisors. DEXCOM 10/2018 – 05/2020 ...
- Apr 19
San Diego, CA
... Supervised and led a team of Research Associates and managed client relationships to deliver FDA approved immunoassays to the clients within budget and time constraints. AZURE Institute, San Diego, CA Oct 2020-Feb 2021 Scientist IV Responsible for ...
- Mar 29
San Diego, CA
... • Project managed overseas clinical trials for patients with cardiovascular and neurodegenerative diseases, outlined safety and efficacy of applied stem cells for treatment, developed required paperwork required by FDA for IND submission, and served ...
- Mar 21
San Diego, CA
... Job Title: CRA/CTA Key Responsibilities: • Performed and coordinated all aspects of the clinical monitoring process in accordance with GCPs, ICH, Title 21, FDA Clinical Research Guidelines and global SOPs. • Assigned to monitor five clinical sites ...
- Mar 10
San Diego, CA
... Conduct pre-launch and launch initiatives prior to and following FDA approval for Praluent (Alirocumab). AstraZeneca Pharmaceuticals LP., Wilmington, DE February 2014 - October 2014 Medical Science Liaison Provided medical and scientific expertise ...
- Mar 07
San Diego, CA, 92129
... • Project managed overseas clinical trials for patients with cardiovascular and neurodegenerative diseases, outlined safety and efficacy of applied stem cells for treatment, developed required paperwork required by FDA for IND submission, and served ...
- Mar 04
San Diego, CA
... 3/16 - 11/16 Zest Dental Solutions - Staff Smart Temporary Assignment Document Control Specialist Updating product labels with DATAMATRIX CODE barcode information with updated UDI 101 information to comply with FDA UDI Rule and Final Rule for FDA ...
- Feb 11
Poway, CA, 92064
... Affairs-Document Control Professional Summary Quality Assurance, Document Control, and Quality systems professional with 10+ years’ experience leveraging broad experience in FDA-regulated pharmaceutical, biomedical, and medical device industries. ...
- Feb 09