| Resume alert | Resumes 21 - 30 of 324 |
Regulatory Compliance Affairs
Dorchester, MA
... in Regulatory Affairs • Relevant coursework: Regulatory Strategy for Product Development, Regulatory Compliance Practice, Introduction to Safety Science, Introduction to FDA Pharma Regulations, Human Experimentation, Lean Concepts and Applications. ... - 2023 Nov 28
... in Regulatory Affairs • Relevant coursework: Regulatory Strategy for Product Development, Regulatory Compliance Practice, Introduction to Safety Science, Introduction to FDA Pharma Regulations, Human Experimentation, Lean Concepts and Applications. ... - 2023 Nov 28
Team Member Medical Devices
Attleboro, MA
... Lemieux *** ****** ****** Seekonk, Massachusetts 02771-5108 Phone: 774-***-**** E-Mail: ad1ek0@r.postjobfree.com Professional Summary: Team member with Engineering to develop new medical devices and improve existing products to meet FDA requirements ... - 2023 Nov 23
... Lemieux *** ****** ****** Seekonk, Massachusetts 02771-5108 Phone: 774-***-**** E-Mail: ad1ek0@r.postjobfree.com Professional Summary: Team member with Engineering to develop new medical devices and improve existing products to meet FDA requirements ... - 2023 Nov 23
Plant Manager Continuous Improvement
Woonsocket, RI
... I have worked with auditing bodies such as AIB, SQF, BRC, and FDA. I am trained in HACCP (certified), FSMA, and food safety programs. I am driven by the challenge of developing people and processes to exceed expectations. Achieving goals and KPI’s ... - 2023 Nov 12
... I have worked with auditing bodies such as AIB, SQF, BRC, and FDA. I am trained in HACCP (certified), FSMA, and food safety programs. I am driven by the challenge of developing people and processes to exceed expectations. Achieving goals and KPI’s ... - 2023 Nov 12
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
Software Development Quality Assurance
Worcester, MA
... Following WSDP and remaining compliant with Quality Assurance, FDA, and participating in customer Audits, ●Computer System Validation/cGMP, setting up brand new UPLC, HPLC, GC systems and instruments. Validating the IQ/OQ/PQ of various systems when ... - 2023 Oct 10
... Following WSDP and remaining compliant with Quality Assurance, FDA, and participating in customer Audits, ●Computer System Validation/cGMP, setting up brand new UPLC, HPLC, GC systems and instruments. Validating the IQ/OQ/PQ of various systems when ... - 2023 Oct 10
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
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