| Resume alert | Resumes 101 - 110 of 288 |
Quality Engineer
Saint Paul, MN
... Strong Knowledge about the FDA regulations, 21 CFR part 820, Part 11 and ISO 14971, 13485. Expertise in risk based sampling and data analysis using Minitab. Performed PPAP, APQP, First Article Inspection (FAIR) and Incoming Inspections. Evaluated ... - 2017 Nov 03
... Strong Knowledge about the FDA regulations, 21 CFR part 820, Part 11 and ISO 14971, 13485. Expertise in risk based sampling and data analysis using Minitab. Performed PPAP, APQP, First Article Inspection (FAIR) and Incoming Inspections. Evaluated ... - 2017 Nov 03
QC Supervisor
Bloomington, MN
... • Participated company audits such as FDA, USDA, CMS, client audits and corporate. • Ensured all supplies and reagents are ordered as needed and no systems are down due to delayed ordering. • Held regular department team meetings and attended ... - 2017 Oct 13
... • Participated company audits such as FDA, USDA, CMS, client audits and corporate. • Ensured all supplies and reagents are ordered as needed and no systems are down due to delayed ordering. • Held regular department team meetings and attended ... - 2017 Oct 13
Sr Engineering Technician
Hennepin County, MN
... Working knowledge of FDA regulations, GMP, ISO13485, 6S and Six Sigma. Hands-on experience in defining validation for systems and processes with proficiency of protocols for equipment and processes. Ability to plan and organize, work effectively and ... - 2017 Oct 02
... Working knowledge of FDA regulations, GMP, ISO13485, 6S and Six Sigma. Hands-on experience in defining validation for systems and processes with proficiency of protocols for equipment and processes. Ability to plan and organize, work effectively and ... - 2017 Oct 02
Mechanical Design Engineer
Minneapolis, MN
... Responsibilities include understanding customer’s needs, generating initial design concept, performing mechanical analysis (FEA, fatigue) and material analysis (biocompatibility, corrosion), conducting GLP study, working with FDA on design intend, ... - 2017 Sep 23
... Responsibilities include understanding customer’s needs, generating initial design concept, performing mechanical analysis (FEA, fatigue) and material analysis (biocompatibility, corrosion), conducting GLP study, working with FDA on design intend, ... - 2017 Sep 23
Sr Chemist
Plymouth, MN
... Expertise in compendia methods from USP, EP, BP and JP as well as GMP, GLP, ICH and FDA and ISO regulatory standards. Advanced computer skills and use of various software applications, and experience with designing DOE. Always works towards ... - 2017 Sep 19
... Expertise in compendia methods from USP, EP, BP and JP as well as GMP, GLP, ICH and FDA and ISO regulatory standards. Advanced computer skills and use of various software applications, and experience with designing DOE. Always works towards ... - 2017 Sep 19
Registered Nurse Customer Service
Dayton, MN, 55327
... understanding of protocols, while adhering SOP, GLP, FDA, USDA, AAALAC, IACUC Work closely with Physicians, study Directors, Veterinarians and study sponsors to ensure studies are conducted according to the SOP's and GLP's Work with physicians and ... - 2017 Sep 19
... understanding of protocols, while adhering SOP, GLP, FDA, USDA, AAALAC, IACUC Work closely with Physicians, study Directors, Veterinarians and study sponsors to ensure studies are conducted according to the SOP's and GLP's Work with physicians and ... - 2017 Sep 19
Medical Device Engineering
Minneapolis, MN
... Experience in GMP, ISO, and FDA controlled environment. Profound knowledge of medical device industry practices, production processes and applicable quality standards Operational knowledge of using MS Office, automated documentation system, ... - 2017 Sep 13
... Experience in GMP, ISO, and FDA controlled environment. Profound knowledge of medical device industry practices, production processes and applicable quality standards Operational knowledge of using MS Office, automated documentation system, ... - 2017 Sep 13
Chemist/Lab Manager/Quality Assurance
Saint Paul, MN
... Valuably promoted changes to laboratory methods, functions, and protocols to ensure FDA and GLP 21 CFR compliance. Effectively performed weekly internal laboratory audits for quality assurance and compliance to current SOP’s and GLP’s. Continually ... - 2017 Sep 05
... Valuably promoted changes to laboratory methods, functions, and protocols to ensure FDA and GLP 21 CFR compliance. Effectively performed weekly internal laboratory audits for quality assurance and compliance to current SOP’s and GLP’s. Continually ... - 2017 Sep 05
Customer Service Sales Associate
Saint Paul, MN, 55114
... Paul, MN July – August 2013 Researched and summarized FDA/ANSI 6236 regulations for medical devices. Completed comprehensive usability analysis and heuristic analysis on the operation of prototype blood analyzers. Sales Associate / Manager On Duty ... - 2017 Aug 29
... Paul, MN July – August 2013 Researched and summarized FDA/ANSI 6236 regulations for medical devices. Completed comprehensive usability analysis and heuristic analysis on the operation of prototype blood analyzers. Sales Associate / Manager On Duty ... - 2017 Aug 29
Cyber Security, HR Generalist, Manager, Consultant, Director, Law
Minneapolis, MN
... I have experience advising corporations on EPA, HIPAA and FDA compliance. I provide litigation management, legal and industry research. I write grants for charter schools, non-profit organizations and scientific research for PhD students at the U of ... - 2017 Aug 08
... I have experience advising corporations on EPA, HIPAA and FDA compliance. I provide litigation management, legal and industry research. I write grants for charter schools, non-profit organizations and scientific research for PhD students at the U of ... - 2017 Aug 08