| Resume alert | Resumes 51 - 60 of 146 |
Management Continuous Improvement
Perry, OH, 44081
... Brief snapshot below: Directed the selection, design, implementation and tracking of regulated (FDA/OSHA/CAPA) Ethical and developmental training programs for plant salaried and hourly personnel aligning with core competencies & WCM and cGMP ... - 2016 Nov 30
... Brief snapshot below: Directed the selection, design, implementation and tracking of regulated (FDA/OSHA/CAPA) Ethical and developmental training programs for plant salaried and hourly personnel aligning with core competencies & WCM and cGMP ... - 2016 Nov 30
Operations Specialist
Cleveland, OH
... Observed all EPA and FDA procedures. Adhered to all DOJ, DOT, OSHA, and ISO 9001 regulations. Training include bio-safety training in BSL2 hood, bio-safety cabinet, PPE, blood borne pathogens, clean room procedures, cold room procedures, and ... - 2016 Oct 05
... Observed all EPA and FDA procedures. Adhered to all DOJ, DOT, OSHA, and ISO 9001 regulations. Training include bio-safety training in BSL2 hood, bio-safety cabinet, PPE, blood borne pathogens, clean room procedures, cold room procedures, and ... - 2016 Oct 05
Data Project
Cleveland, OH
... Experience working in an FDA regulated environment, with excellent understanding of cGxP (cGCP, cGMP, cGDP, cGLP) and Standard Operating Procedure (SOP) and in preparing documentation which is in compliance with 21 CFR Part 11. Detail oriented and a ... - 2016 Aug 01
... Experience working in an FDA regulated environment, with excellent understanding of cGxP (cGCP, cGMP, cGDP, cGLP) and Standard Operating Procedure (SOP) and in preparing documentation which is in compliance with 21 CFR Part 11. Detail oriented and a ... - 2016 Aug 01
High School Safety
Beachwood, OH, 44122
... -Able to read complex diagrams and written procedures, needed to assemble various hospital scanners -Proficiency with wiring diagrams -Experienced with preparing for internal and Food and Drug Administration (FDA) audits, including but not limited ... - 2016 May 16
... -Able to read complex diagrams and written procedures, needed to assemble various hospital scanners -Proficiency with wiring diagrams -Experienced with preparing for internal and Food and Drug Administration (FDA) audits, including but not limited ... - 2016 May 16
Engineer Project Manager
Cleveland, OH
... Implemented knowledge of CGMP, OSHA, EPA and FDA facility requirements and regulations. Utilized knowledge of chemistry, statistics, equipment design, cost estimation, process control and process scale-up. Required to use of knowledge of sterile ... - 2016 Apr 29
... Implemented knowledge of CGMP, OSHA, EPA and FDA facility requirements and regulations. Utilized knowledge of chemistry, statistics, equipment design, cost estimation, process control and process scale-up. Required to use of knowledge of sterile ... - 2016 Apr 29
Assistant Research
Cleveland, OH
... repair (Biobandage™) • Contributed towards the development of an assay for Human Platelet Lysate (PLUS™ ) to meet requirements for FDA • Generated scientific data to support (PLUS™ ) as a favorable substitute for animal derived serum • Posses an ... - 2016 Jan 23
... repair (Biobandage™) • Contributed towards the development of an assay for Human Platelet Lysate (PLUS™ ) to meet requirements for FDA • Generated scientific data to support (PLUS™ ) as a favorable substitute for animal derived serum • Posses an ... - 2016 Jan 23
Engineer
Painesville, OH
... organized the return of faulty testers to the vendor oAudited Finished dispensers for function & cosmetic appeal Knowledgeable of FDA Current Good Manufacturing Practices (cGMP) 6/2009 - 11/2012 GOJO Industries Cuyahoga Falls, Ohio Quality Control ... - 2015 Dec 14
... organized the return of faulty testers to the vendor oAudited Finished dispensers for function & cosmetic appeal Knowledgeable of FDA Current Good Manufacturing Practices (cGMP) 6/2009 - 11/2012 GOJO Industries Cuyahoga Falls, Ohio Quality Control ... - 2015 Dec 14
Java Developer Test Cases
Cleveland, OH
... Approved by the FDA, it is used by the Lab technicians to enter information as well as connect it to instruments in the lab so that the results from the tests performed by the instruments are automatically entered into the Commercial Laboratory ... - 2015 Sep 18
... Approved by the FDA, it is used by the Lab technicians to enter information as well as connect it to instruments in the lab so that the results from the tests performed by the instruments are automatically entered into the Commercial Laboratory ... - 2015 Sep 18
Medical Mechanical Engineering
Cleveland, OH
... have knowledge of FDA 510(k), 21 CFR 820, ISO 13485, and six sigma yellow belt trained. Strong skills at technical writing and results presentations. Patent writing Experiences. Proposals and reports writing experiences. 1/2 BOLAN LI 2123 Martin ... - 2015 Jun 25
... have knowledge of FDA 510(k), 21 CFR 820, ISO 13485, and six sigma yellow belt trained. Strong skills at technical writing and results presentations. Patent writing Experiences. Proposals and reports writing experiences. 1/2 BOLAN LI 2123 Martin ... - 2015 Jun 25
Validation Engineer
Cleveland, OH
... EXPERIENCE Verification and Validation Engineer, Philips Healthcare, Highland Heights, OH (9/2008 – 9/2014) Participated in new medical device and installed based projects including planning, execution, and reporting in a FDA environment. ... - 2015 May 16
... EXPERIENCE Verification and Validation Engineer, Philips Healthcare, Highland Heights, OH (9/2008 – 9/2014) Participated in new medical device and installed based projects including planning, execution, and reporting in a FDA environment. ... - 2015 May 16