| Resume alert | Resumes 21 - 30 of 82 |
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
Plant Manager Safety
North Kingstown, RI
... Secret Security Clearance Certifications: OSHA 11 Additional training: DOT training, Safety Training, Leadership, Basic Life Support, FDA PROFESSIONAL BACKGROUND Airgas Northeast, East Greenwich, RI 2017 - Present Distribution Manager (2017 – ... - 2020 Aug 07
... Secret Security Clearance Certifications: OSHA 11 Additional training: DOT training, Safety Training, Leadership, Basic Life Support, FDA PROFESSIONAL BACKGROUND Airgas Northeast, East Greenwich, RI 2017 - Present Distribution Manager (2017 – ... - 2020 Aug 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
Manager Training
West Warwick, RI, 02893
... The validation package presented to the FDA during the PAI and was highly commended by the agency. Client satisfaction commended us with the Development of the Validation Master Plan for the new site. Project Manager for validation projects on ... - 2019 Dec 26
... The validation package presented to the FDA during the PAI and was highly commended by the agency. Client satisfaction commended us with the Development of the Validation Master Plan for the new site. Project Manager for validation projects on ... - 2019 Dec 26
Operations/Quality
Cranston, RI
... Maintain the Technology Roadmap, Negotiate capital equipment procurement, Conflict Minerals Reporting, Diversified background in operations, RoHS compliance, ISO Management Systems 9001:2015, AS9100, 27001, 13485:2015, Auditing, cGMP/FDA Regulatory ... - 2019 Dec 26
... Maintain the Technology Roadmap, Negotiate capital equipment procurement, Conflict Minerals Reporting, Diversified background in operations, RoHS compliance, ISO Management Systems 9001:2015, AS9100, 27001, 13485:2015, Auditing, cGMP/FDA Regulatory ... - 2019 Dec 26
Recent Biomedical Engineering Graduate
Norton, MA
... 3 groups of up to 10-12 students, tutoring over 30 students in physics and math TECHNICAL SKILLS: Knowledgable in FDA patent regulation and classification procedures Proficient with Microsoft Office, LabVIEW, Solidworks, Minitab 18 and Mathcad. ... - 2019 May 15
... 3 groups of up to 10-12 students, tutoring over 30 students in physics and math TECHNICAL SKILLS: Knowledgable in FDA patent regulation and classification procedures Proficient with Microsoft Office, LabVIEW, Solidworks, Minitab 18 and Mathcad. ... - 2019 May 15
Manager Project Director, IT
West Warwick, RI
... Specialties include: strategic planning, compliance/regulations (cGMP and FDA), planning and budgeting, IT Governance, V & V life cycle requirements (SDLC), Change Management, Document Control and Project and Human Resource management. SKILLS AND ... - 2019 Apr 17
... Specialties include: strategic planning, compliance/regulations (cGMP and FDA), planning and budgeting, IT Governance, V & V life cycle requirements (SDLC), Change Management, Document Control and Project and Human Resource management. SKILLS AND ... - 2019 Apr 17