| Resume alert | Resumes 1 - 10 of 337 |
Manufacturing Associate Customer Service
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
... - 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
Research Scientist Senior
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
... 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
Associate Director Quality Assurance
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
... • 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
United States Clinical Research
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
... 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
Medical Affairs professional
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
... 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
Research Director, Pharmaceutical Sales
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
... • 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
Technical Writer Data Management
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
... 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
Quality Assurance Document Control
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
... 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
Supply Chain Senior Buyer
San Diego, CA
... •Worked within ISO 9001 guidelines and under FDA 13485. BIT MEDTECH-San Diego, California Contract Manufacturer of Medical Devices Product Line Manager/Senior Buyer July 2010 - July 2014 •Managed a Medical Device Production line and was responsible ... - Feb 05
... •Worked within ISO 9001 guidelines and under FDA 13485. BIT MEDTECH-San Diego, California Contract Manufacturer of Medical Devices Product Line Manager/Senior Buyer July 2010 - July 2014 •Managed a Medical Device Production line and was responsible ... - Feb 05
Quality Assurance Software
El Cajon, CA, 92019
... System Test Engineer Jul 2019-Apr 2020 Philips Health (SSI) San Diego, CA •Created FDA approved test cases based upon the product requirements and stories using HP/MF-ALM (Quality Center). •Tested the various FDA class 1 and class 2 devices such as ... - Feb 05
... System Test Engineer Jul 2019-Apr 2020 Philips Health (SSI) San Diego, CA •Created FDA approved test cases based upon the product requirements and stories using HP/MF-ALM (Quality Center). •Tested the various FDA class 1 and class 2 devices such as ... - Feb 05