| Resume alert | Resumes 21 - 30 of 119 |
Clinical Research Medical
Plymouth, MA
... Analysis • Ability to recognize and apply regulatory requirements for clinical research (particularly requirements of the FDA) • Ability to read, analyze and critique clinical research literature • Strong knowledge of relevant drugs, chemical ... - 2021 Apr 09
... Analysis • Ability to recognize and apply regulatory requirements for clinical research (particularly requirements of the FDA) • Ability to read, analyze and critique clinical research literature • Strong knowledge of relevant drugs, chemical ... - 2021 Apr 09
Assistant Document Control
Norwood, MA
... FDA and ICH guidelines; the roles of CRA and CRC; the types of monitoring visits; the role of IRBs; Safety, Accountability, and Regulatory Compliance. Northeastern University, Level Program, Online Introduction to Data Analytics November 2018- ... - 2020 Dec 12
... FDA and ICH guidelines; the roles of CRA and CRC; the types of monitoring visits; the role of IRBs; Safety, Accountability, and Regulatory Compliance. Northeastern University, Level Program, Online Introduction to Data Analytics November 2018- ... - 2020 Dec 12
Engineer Medical Device
Attleboro, MA
... I have worked in product development, testing, and the FDA design controls process, specifically in the spine and sports medicine sections of the industry. I am an outgoing and driven professional with a strong passion for technical problem solving ... - 2020 Dec 10
... I have worked in product development, testing, and the FDA design controls process, specifically in the spine and sports medicine sections of the industry. I am an outgoing and driven professional with a strong passion for technical problem solving ... - 2020 Dec 10
Chemical Technician
Swansea, MA
... Manufacturing Responsibilities and functions included large scale manufacturing of APIs, operation of chemical equipment, adherence to cGMP, DEA, and FDA guidelines, resolving production issues by independent troubleshooting and root-cause analysis. ... - 2020 Dec 04
... Manufacturing Responsibilities and functions included large scale manufacturing of APIs, operation of chemical equipment, adherence to cGMP, DEA, and FDA guidelines, resolving production issues by independent troubleshooting and root-cause analysis. ... - 2020 Dec 04
Manager Medical
Plymouth, MA
... I was responsible for the GRAS affirmation of the new alkyd by the FDA. I developed a range of ingredients based on the alkyd structure into a full range of zero-saturated-fat products with “pseudoplastic” structure (margarines, frostings, icings, ... - 2020 Nov 19
... I was responsible for the GRAS affirmation of the new alkyd by the FDA. I developed a range of ingredients based on the alkyd structure into a full range of zero-saturated-fat products with “pseudoplastic” structure (margarines, frostings, icings, ... - 2020 Nov 19
Chemical Engineering Medical Device
Providence, RI
... •Extensive knowledge and experience in validating computer systems following the Software Development Life Cycle (SDLC) as per FDA regulations and cGXP (GLP/GCP/GMP) guidelines. •Data Integrity on the CSV audits per the ALCOA© thumb rules. •Familiar ... - 2020 Nov 04
... •Extensive knowledge and experience in validating computer systems following the Software Development Life Cycle (SDLC) as per FDA regulations and cGXP (GLP/GCP/GMP) guidelines. •Data Integrity on the CSV audits per the ALCOA© thumb rules. •Familiar ... - 2020 Nov 04
Quality Engineer Manager
Attleboro, MA
... 21 CFR Part 820 • CFR 21, Part 803 Medical Device Adverse Event Reporting • CFR 21, Part 806 Field Action Decisions • FDA 483 Response Experience • Process Validation – IQ, OQ & PQ • GMP – Good Manufacturing Practices • CAPA and Complaint ... - 2020 Sep 12
... 21 CFR Part 820 • CFR 21, Part 803 Medical Device Adverse Event Reporting • CFR 21, Part 806 Field Action Decisions • FDA 483 Response Experience • Process Validation – IQ, OQ & PQ • GMP – Good Manufacturing Practices • CAPA and Complaint ... - 2020 Sep 12
Chief Administration Officer
North Providence, RI
... Regulatory liaison for cGMP compliance, FDA regulatory compliance, and ISO 9000 quality system registration and recertification. The Custom Device Certification was a key contribution. This certification was the basis for spinning off two sister ... - 2020 Sep 10
... Regulatory liaison for cGMP compliance, FDA regulatory compliance, and ISO 9000 quality system registration and recertification. The Custom Device Certification was a key contribution. This certification was the basis for spinning off two sister ... - 2020 Sep 10
Project Manager
Providence, RI
... Supported international and domestic FDA inspections by retrieving the required data for a variety of regulatory agencies. Assisted in managing and updating global Records Retention Schedule in SharePoint to remain compliant in 60+ countries. ... - 2020 Sep 07
... Supported international and domestic FDA inspections by retrieving the required data for a variety of regulatory agencies. Assisted in managing and updating global Records Retention Schedule in SharePoint to remain compliant in 60+ countries. ... - 2020 Sep 07
Engineer Design
Dartmouth, MA, 02747
... Insured illumination safety compliance: FDA radiological hazards Performed tests on MTF, DOF (focus depth), magnification, optical resolution, etc. TOBIAS ASSOCIATES: Spectrophotometer engineer 2/96-10/96 Designed and built a hand-held ... - 2020 Mar 12
... Insured illumination safety compliance: FDA radiological hazards Performed tests on MTF, DOF (focus depth), magnification, optical resolution, etc. TOBIAS ASSOCIATES: Spectrophotometer engineer 2/96-10/96 Designed and built a hand-held ... - 2020 Mar 12