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FDA resumes in New Haven, CT

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Resume alert Resumes 31 - 40 of 93

Biomedical Engineer

Portland, CT
... Exercised functions requiring knowledge of ISO/FDA/ASTM regulations for medical devices. Complied data including hardware test data, environmental values, and shipping/receiving data by assembly components into comprehensive FEMA and MTBF analyses. ... - 2020 Apr 15

Quality engineer

New Haven, CT
Ranjit Parajuli (US Citizen) 203-***-**** adcs5u@r.postjobfree.com Skills ISO 9001, ISO13485, FDA QMS, EPR, BPCS CAPA, FMEA SPC, SOP, STP CGMP, GLP, 5s/6s, MSDS Empower, LIMS Microsoft office Assay, Western Blots HPLC, UV, FTIR Dissolution, ... - 2020 Apr 14

Engineer Customer Service

Milford, CT
... for Medtronic’s Minimally Invasive Therapies Group (MITG) Investigated and determined reportability of complaints to FDA and/or other international regulatory agencies Assessed complaint records and identified appropriate internal department ... - 2020 Apr 13

Mechanical Power

Waterbury, CT
... SKILLS Microsoft Office, Excel, and Word Lean Manufacturing Protocol Experienced in SAP Read schematics, blueprints and drawings Compliant with FDA and ISO requirements Well-organized Skilled with hand tools and power tools Work independently or in ... - 2019 Sep 04

Principle Consultant

Milford, CT
... Management Computer Validation EDMS Administration Software Integration Change Control Technical Writing Application Support FDA 21 CFR Part 11 Business Liaison Regulatory Publishing Document Management SDLC Professional Experience 2018 – Present ... - 2019 Apr 05

Director of Operations and Logistics

Bridgeport, CT
... Standard Operating Procedures Perform and document scheduled inspections to ensure warehouse and transportation operations are within FDA and OSHA compliance Collaborate with IT Department on systems integration and technology upgrades Director of ... - 2018 Nov 05

Biomedical Engineer

New Haven, CT
... ● Prepared and assembled laboratory equipment to comply with cGMP and GLP specification recommended for FDA class-II device quality assurance. ● Performed Equipment Qualification and tracked calibration to comply with ISO-13485 QMS. ● Reviewed ... - 2018 Sep 17

Vp of Manufacturing and Supply Chain

Branford, CT
... Core competencies include: Strategy and Execution Operations Optimization Risk Management P&L / Capital Budget Management KPI Improvement Strategist Change Management Quality Systems FDA / cGMP Regulatory Compliance New Product / Portfolio ... - 2018 Aug 26

Engineering Assistant

Bridgeport, CT
... AREA OF EXPERTIES Process/design Validation and Verification regulations FDA/GMP Requirements Incident management- CAPA guidelines 21 CRF Part 11 Documentation with International Standards Aseptic conditions/Clean room practice Pro/Engineer & Solid ... - 2018 Aug 22

Professor of Medicine, Laboratory Director

New Haven, CT
... Follow and enforce good tissue practice guidelines HC/TTP as mandated by recent FDA regulations. Experience with FDA tissue regulations and process equipment qualification and validation. Facilitate scheduling for oocyte retrievals, embryo culture, ... - 2018 Aug 18
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