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Resumes 31 - 40 of 96 |
Shelton, CT
... Initialize paper Work for FDA in the medical field and ISO requirements. •CNC programming 3, 4 & 5 axis Mills •CNC programming Turn/mill Lathes •CNC programming Swiss style lathes •Supervision •Budget planning •Lean Manufacturing Training /Value ...
- 2020 Jun 11
Trumbull, CT
... Swedish Match, Inc., Owensboro, KY January 2009 to March 2011 Successfully managed PMO efforts, using deep COT knowledge, to select and implement ERP & CRM systems for this multi-national enterprise, allowing for fulfillment of FDA traceability and ...
- 2020 Apr 29
Southington, CT
... Ensures USDA, FDA label compliance Receive and verify ongoing certificates of analyses and specifications Sample collection and testing: Maintain data and submit samples for extensive microbiological testing. Execute sample collection and submittals ...
- 2020 Apr 17
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
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
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
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
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
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
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