| Resume alert | Resumes 1 - 10 of 190 |
Project Management High School
Minneapolis, MN
... Implement GMP in the food industry as well as SOPs, HACCP, FDA regulation. Routinely monitor quality issues from production in a controlled manner. Daily tasks included product analysis cook, test, NIR, destiny, and moisture test. Personal ... - May 19
... Implement GMP in the food industry as well as SOPs, HACCP, FDA regulation. Routinely monitor quality issues from production in a controlled manner. Daily tasks included product analysis cook, test, NIR, destiny, and moisture test. Personal ... - May 19
Quality Assurance Customer Support
Crystal, MN
... Wrote FDA quality procedures and training programs for all areas in the optical laboratory and structure and maintain a high level of quality system. Analyzed business situations, production capabilities, manufacturing problems, economic trends, ... - May 18
... Wrote FDA quality procedures and training programs for all areas in the optical laboratory and structure and maintain a high level of quality system. Analyzed business situations, production capabilities, manufacturing problems, economic trends, ... - May 18
Data Entry Quality Technician
Minneapolis, MN
Patricia Williams Skills: ●Reading blueprints ●Using microscope, soldering and adhesive bonding, ●SOP, ISO and FDA requirements ●Quality assurance ●Clean room ●Data entry ●GD&T ●PPAP ●Measurement tools (Mics, height stand, gauges and caliper) ●Basic ... - May 14
Patricia Williams Skills: ●Reading blueprints ●Using microscope, soldering and adhesive bonding, ●SOP, ISO and FDA requirements ●Quality assurance ●Clean room ●Data entry ●GD&T ●PPAP ●Measurement tools (Mics, height stand, gauges and caliper) ●Basic ... - May 14
Business Analyst Project Manager
Minneapolis, MN
... resources Facilitated analysis for several hundred reports considering validation and verification processes dependent upon FDA guidelines TLC Companies, Brooklyn Center, Minnesota Business Analyst/Project Manager, 2015-2018 Developed functional ... - Apr 18
... resources Facilitated analysis for several hundred reports considering validation and verification processes dependent upon FDA guidelines TLC Companies, Brooklyn Center, Minnesota Business Analyst/Project Manager, 2015-2018 Developed functional ... - Apr 18
Human Factors User Experience
Minneapolis, MN
... I have extensive experience designing for the regulatory rigor of FDA medical device validation (AAMI Human Factors certification) and designing/auditing for compliance with WCAG 2.0/2.1 compliance (WebAIM Accessibility Certification). Medtronic ... - Apr 17
... I have extensive experience designing for the regulatory rigor of FDA medical device validation (AAMI Human Factors certification) and designing/auditing for compliance with WCAG 2.0/2.1 compliance (WebAIM Accessibility Certification). Medtronic ... - Apr 17
Document Control Medical Device
Maple Grove, MN
... ● Followed FDA compliance and good manufacturing practices. ● Actively take part in Internal audit at other facilities/Divisions ● Gather and report various performance metrics for quarterly Management Review meetings. - Apr 16
... ● Followed FDA compliance and good manufacturing practices. ● Actively take part in Internal audit at other facilities/Divisions ● Gather and report various performance metrics for quarterly Management Review meetings. - Apr 16
Supply Chain Project Manager
Plymouth, MN
... • Notable skills: CAPA (Corrective and Preventive Actions), RCA (Root Cause Analysis), ERP-Oracle, PLM- Agile, ISO 13485, ISO 14971, and FDA 21 CFR 820 cGMP. SMITHS MEDICAL Plymouth MN Data Management Analyst (Contract) March 2015 to September 2016 ... - Apr 15
... • Notable skills: CAPA (Corrective and Preventive Actions), RCA (Root Cause Analysis), ERP-Oracle, PLM- Agile, ISO 13485, ISO 14971, and FDA 21 CFR 820 cGMP. SMITHS MEDICAL Plymouth MN Data Management Analyst (Contract) March 2015 to September 2016 ... - Apr 15
Medical Devices Clinical Research
Maple Grove, MN
... SPECIAL INTEREST AND RESEARCH •(510), PMA submissions of class II and III medical devices to FDA. •FDA regulatory standards, QSR, 21 CFR 830, ISO 13485. •Molecular, Biological research and techniques. •Biocompatibility testing. •Cell Culture ... - Apr 13
... SPECIAL INTEREST AND RESEARCH •(510), PMA submissions of class II and III medical devices to FDA. •FDA regulatory standards, QSR, 21 CFR 830, ISO 13485. •Molecular, Biological research and techniques. •Biocompatibility testing. •Cell Culture ... - Apr 13
Funeral Director Service Coordinator
Minneapolis, MN
... partners regarding tissue cases ● CTBS certified ● Packing and handing tissue and research tissue in accordance with the FDA ● Practice sterile procedures with procurement ● Packaging and Labeling tissue grafts in accordance with SOPs ● Handling ... - Apr 10
... partners regarding tissue cases ● CTBS certified ● Packing and handing tissue and research tissue in accordance with the FDA ● Practice sterile procedures with procurement ● Packaging and Labeling tissue grafts in accordance with SOPs ● Handling ... - Apr 10
Sterile Processing Technician
Minneapolis, MN
... Followed OSHA, FDA and AAMI guidelines related to sterilization in compliance with administrative regulations. STERILE PROCESSING TECHNICIAN 08/2019 to 11/2021 Methodist Hospital 6500 Excelsior Blvd 55426 e Wrapped trays, instrument packs, and sets. ... - Mar 23
... Followed OSHA, FDA and AAMI guidelines related to sterilization in compliance with administrative regulations. STERILE PROCESSING TECHNICIAN 08/2019 to 11/2021 Methodist Hospital 6500 Excelsior Blvd 55426 e Wrapped trays, instrument packs, and sets. ... - Mar 23