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Resumes 61 - 70 of 179 |
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
Chaska, MN, 55318
... Process Improvement Organization Change Management Manufacturing Planning Compliance ITAR / FDA / CAPA Quality Management ISO9001 ISO13485 Lean Manufacturing Program and Project Management Cross Functional Team Leadership Performance Management Risk ...
- 2017 Oct 03
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
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
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
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
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
Burnsville, MN
... Work with management team on FDA, USDA, and DOV audits. Perform GMP audits on production floor and fill out CAPA forms as needed. Monitor production area for routine microbiological testing. Currently on the Listeria Teamwho works to minimize the ...
- 2017 Aug 02
Minneapolis, MN
... Have supported Trackwise system also which is a complaint management system which is a critical application reporting to FDA. Handling the Data Warehouse interface between application and DWH database and responsible for fixing in case of any ...
- 2017 Jul 21
Maple Grove, MN
... Ensured batching procedures were followed accurately Promoted food safety and employee safety during processing Knowledge of FDA, SSOP’s, GMP’s and HACCP procedures Production Supervisor & Formulation Supervisor 2001 to 2006 Jennie-O Turkey Store, ...
- 2017 Jul 17