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FDA resumes in Plymouth, MI, 48170

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Resume alert Resumes 91 - 100 of 178

Manager Management

West Bloomfield Township, MI
... - R F implementation • General Motors MGO - CLIPS / SMART /DDL • Andon / Pick to Light systems • Exacta / Kronos / GMTKS timekeeping systems • SAP / I2 Transportation solutions • AIB, Silliker, FDA, HACCP, BRC, and HAZMAT Compliance/Certification. ... - 2016 Feb 21

Project Manager Management

Plymouth, MI, 48170
... Applications (IND) which are components of investigational and market registration documents for Food and Drug Administration (FDA) PROQUEST, Ann Arbor, Michigan, 2008 – 2009 (ProQuest creates specialized information resources and technologies that ... - 2016 Feb 16

Sales Manager

Ann Arbor, MI
... Clinical Trial and Engineering Manager August 2014-February 2015 Authored protocols and case report forms necessary for executing FDA clinical trials Negotiated contacts and budgets with hospital’s research staff for FDA clinical trials Owned client ... - 2016 Jan 28

Sales Management

Ann Arbor, MI
... Oversee all hospital contracting of blood products and services, sales strategy planning, team development, sales production forecasting, and continuing education development for staff and customer base, ensuring full compliance with FDA regulations ... - 2016 Jan 28

Maintenance Supervisor Engineer

Ann Arbor, MI
... Maintained equipment per GMP and ISO 13485 FDA 21, CFR part 280 for Class I and Class II medical devices and products. Worked closely with manufacturing needs & resolved issues on a daily basis. Handle all complaints, grievances & discipline as ... - 2015 Oct 19

Manager Management

Wixom, MI
... Packets, Letter of guarantee, Prop 65 Statement, etc.) Customer Complaints and Trending Analysis Regulatory Requirements (FDA, MDA, USDA, etc.) USDA Traces Audits (BRC, Organic, SQF, USDA, FDA/MDA, and Customer) Corrective/Preventive Action and ... - 2015 Oct 12

Quality Control Management

Detroit, MI
... Science major with a dual background of industry and hands on experience in research laboratory, which provided thorough knowledge of cGMP, GLP, FDA regulatory guidance, ICH, ISO and USP guidelines and requirements of ANDA submissions. ... - 2015 Aug 25

Office Consultant

Livonia, MI, 48152
... Performed reporting, validation and documentation in compliance with FDA Extensively used SAS/Macro facility to provide reusable programs that can be conveniently used time to time. Produced quality customized reports by using PROC TABULATE, PROC ... - 2015 Jun 25

Manager Quality

Bloomfield Hills, MI
... managed all aspects of QA, APQP / PPAP and RA (FDA QSR) at 12 NAFTA plants, . developed and implemented a state of the art documented Quality Management System, . accomplished ISO 9001, ISO/TS 16949, ISO 13485 and AS9100C certifications and IQ/OQ/PQ ... - 2015 Jan 27

Quality Control Supervisor

Walled Lake, MI
... Familiar with compliance specifications within SOP, cGMP, GLP guideline, controlled substances and FDA regulations. Ability to perform qualitative and quantitative analysis of in-process, finished, and stability products using instruments such as ... - 2014 Dec 13
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