| Resume alert | Resumes 31 - 40 of 525 |
Clinical Trial Research
Boston, MA
... Answered FDA statistical related questions Developed an automated program for meta-analysis of KM survival curve, saved biostatistician 80% time Data Scientist at Flagship Pioneering (Moderna founding VC) 2018.2 – 2019.1 Cambridge, MA Quantitative ... - 2023 Nov 20
... Answered FDA statistical related questions Developed an automated program for meta-analysis of KM survival curve, saved biostatistician 80% time Data Scientist at Flagship Pioneering (Moderna founding VC) 2018.2 – 2019.1 Cambridge, MA Quantitative ... - 2023 Nov 20
Quality control inspector
Wakefield, MA, 01880
... Ensured on a daily basis that quality records and company practices are compliant with FDA's Quality System Regulation (QSR), and internal procedures and regulations. Reviewed associated paperwork, completed inspection records using Good ... - 2023 Nov 17
... Ensured on a daily basis that quality records and company practices are compliant with FDA's Quality System Regulation (QSR), and internal procedures and regulations. Reviewed associated paperwork, completed inspection records using Good ... - 2023 Nov 17
Food Safety Quality Control
Ipswich, MA, 01938
... Drafted detailed reports for improved communication between local officials, MA DMF, and FDA. Enforced local and state rules for safe shellfish harvest in line with regulations. CMS Consulting; Milford, MA 2005 - 2009 Freelance Consultant Guided ... - 2023 Nov 09
... Drafted detailed reports for improved communication between local officials, MA DMF, and FDA. Enforced local and state rules for safe shellfish harvest in line with regulations. CMS Consulting; Milford, MA 2005 - 2009 Freelance Consultant Guided ... - 2023 Nov 09
Business Development Product Delivery
Newton, MA
... -Led compounding pharmacy operations, ensuring strict cGMP, FDA, and DEA compliance. -Successfully guided FDA audits, showcasing strong regulatory adherence. -Established a culture of compliance and proactive risk management. -Optimized ... - 2023 Oct 12
... -Led compounding pharmacy operations, ensuring strict cGMP, FDA, and DEA compliance. -Successfully guided FDA audits, showcasing strong regulatory adherence. -Established a culture of compliance and proactive risk management. -Optimized ... - 2023 Oct 12
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
Research Scientist Quality Control
Foxborough, MA
... Actively involved in preparation of Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) documents and Bioburden evaluation for FDA approval Protein purification and validation of purity Performing ... - 2023 Sep 22
... Actively involved in preparation of Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) documents and Bioburden evaluation for FDA approval Protein purification and validation of purity Performing ... - 2023 Sep 22
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
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