| Resume alert | Resumes 41 - 50 of 585 |
Team Member Sql Server
Needham, MA
... Analyzed, maintained, and go over test documents to meet 21 CFR 820 (FDA QSR) and ISO requirements. Manually generated and implemented templates for Test plan, Test Cases, and Test Scripts and performed Testing on the entire application. Worked ... - 2023 Oct 03
... Analyzed, maintained, and go over test documents to meet 21 CFR 820 (FDA QSR) and ISO requirements. Manually generated and implemented templates for Test plan, Test Cases, and Test Scripts and performed Testing on the entire application. Worked ... - 2023 Oct 03
Equity Analyst
Belmont, MA
... For pharmaceutical companies I review the FDA calendar and read industry publications to identify investment candidates. I analyze Phase I, II, III studies to examine the efficacy of the drug and assess the likelihood of FDA approval. I review ... - 2023 Oct 02
... For pharmaceutical companies I review the FDA calendar and read industry publications to identify investment candidates. I analyze Phase I, II, III studies to examine the efficacy of the drug and assess the likelihood of FDA approval. I review ... - 2023 Oct 02
Data Analyst Management
Jamaica Plain, MA
... Proficient in healthcare data management and analysis, with experience in Medical Device Reporting to the FDA. Prepared and analyzed data regularly for reports, actively participated in team discussions and project management. Utilized Microsoft ... - 2023 Sep 19
... Proficient in healthcare data management and analysis, with experience in Medical Device Reporting to the FDA. Prepared and analyzed data regularly for reports, actively participated in team discussions and project management. Utilized Microsoft ... - 2023 Sep 19
Associate Scientist Analytical
Grafton, MA, 01519
... Faced regulatory audits with agencies like US-FDA, WHO and FDA-Thailand. Core competencies Ability to maintain lab with minimal supervision, attention to detail and handle pressure during high priority projects with effective stakeholder management ... - 2023 Sep 18
... Faced regulatory audits with agencies like US-FDA, WHO and FDA-Thailand. Core competencies Ability to maintain lab with minimal supervision, attention to detail and handle pressure during high priority projects with effective stakeholder management ... - 2023 Sep 18
Chemical tech
Medway, MA, 02053
... - Weymouth, MA 2012 to 2014 Inspection and clean to FDA regulations of machinery before and after any runs ! Pump up a liquid to top of tank which then gets pushed through a nozzle to make a very fine spray which on the way down would contact ... - 2023 Sep 17
... - Weymouth, MA 2012 to 2014 Inspection and clean to FDA regulations of machinery before and after any runs ! Pump up a liquid to top of tank which then gets pushed through a nozzle to make a very fine spray which on the way down would contact ... - 2023 Sep 17
Clinical Research Public Health
Newton, MA
... • Demonstrated extensive knowledge of regulatory requirements governing clinical research, including FDA regulations, Clinical Trial Management System (CTMS), Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, ... - 2023 Aug 31
... • Demonstrated extensive knowledge of regulatory requirements governing clinical research, including FDA regulations, Clinical Trial Management System (CTMS), Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, ... - 2023 Aug 31
Quality Assurance Supply Chain
Norwood, MA
... • Managed the reconciliation of method development and validation, GLP compliance, documentation, completeness, and compliance per FDA guidelines, following SOPs, protocols, QA compliance, and a review checklist. Academic Project • Conducted a ... - 2023 Aug 29
... • Managed the reconciliation of method development and validation, GLP compliance, documentation, completeness, and compliance per FDA guidelines, following SOPs, protocols, QA compliance, and a review checklist. Academic Project • Conducted a ... - 2023 Aug 29
Supply Chain Operations Manager
Medford, MA
... Quality and Supplier Qualifications and ISO 9001-2015 and FDA 13485 certifications audits. Persimmon Technologies Wakefield, MA June 2014 – June 2016 Senior Material Program Manager Materials Program Manager for Robotics manufacturer supporting the ... - 2023 Aug 07
... Quality and Supplier Qualifications and ISO 9001-2015 and FDA 13485 certifications audits. Persimmon Technologies Wakefield, MA June 2014 – June 2016 Senior Material Program Manager Materials Program Manager for Robotics manufacturer supporting the ... - 2023 Aug 07
Product development engineer
Lowell, MA
... Recall Technician - Temporary Nova Biomedical - Billerica, MA September 2013 to November 2013 Involved in a regulatory compliant FDA recall of blood glucose test strips. Initiated RMA log sheets by confirming consumer demographics and expected ... - 2023 Jul 21
... Recall Technician - Temporary Nova Biomedical - Billerica, MA September 2013 to November 2013 Involved in a regulatory compliant FDA recall of blood glucose test strips. Initiated RMA log sheets by confirming consumer demographics and expected ... - 2023 Jul 21
Drug Safety Specialist
Boston, MA
... ● Process Individual Case Study Reports (ICSR) and serious adverse event (SAE) reports including case intake, duplicate check, data entry, generation of narratives, MedDRA coding, quality checks, submissions to FDA through gateway; ● Submission of ... - 2023 Jul 10
... ● Process Individual Case Study Reports (ICSR) and serious adverse event (SAE) reports including case intake, duplicate check, data entry, generation of narratives, MedDRA coding, quality checks, submissions to FDA through gateway; ● Submission of ... - 2023 Jul 10