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Resume alert |
Resumes 71 - 80 of 150 |
Detroit, MI
... Skills UV Spectrometer Method Validation MS Office tools FDA Compliance INDUSTRIAL EXPERIENCE Graduate Research Assistant Michigan Tech Houghton MI April 2016-April 2017 Employed GLP to conduct routine analytical testing and instrumental analysis. ...
- 2017 Jun 19
West Bloomfield Township, MI
... process, team focused improvements, & manufacturing cross-walks Harmonized NA and global quality systems Launched aggressive APQP program for new product introduction TPS/ATOMS Leader Special assignments for FDA and Medical plastic processing. ...
- 2017 Jun 15
Farmington, MI, 48331
... various salty snacks on 3 production lines • Meet service to sales daily production targets • Performed OHSA, USDA and FDA cGMP compliance Audit EDUCATION MBA in Finance New York University - New York, NY Economics London School of Economics - ...
- 2017 Jun 02
Grosse Pointe, MI, 48236
... Food and Drug Administration (FDA); Code of Federal Regulations (CFR) Processed request for country of origin, quotes and duty rates for shipping purposes. Track and trace shipments for estimated time of arrival; resolve any shipping issues that may ...
- 2017 Apr 28
Inkster, MI
... The facility was quality associated with FDA house rules and regulations in which I gained knowledge, and experience in quality associated with the daily job operations. Agent / Partner Primerica Financial Services - Southfield, MI - March 2003 to ...
- 2017 Apr 17
Canton, MI
... 16 Created Test Method Validations, Process Validation, IQ, OQ, and PQ with documentation under FDA Remediation. Authored Technical Review for drawing, part inspection plan, manufacturing & service work instruction with cross-functional team. ...
- 2017 Feb 09
Windsor, ON, N9H 2M9, Canada
... Knowledge of safety and quality regulations, WHMIS, ISO, EPA, FDA as well as GMP. Knowledgeable in software applications such as Microsoft Office, LIMS, ChemDraw and LabView. Possess excellent organizational, time management and multi-tasking skills ...
- 2016 Dec 06
Allen Park, MI
... Shortly after my arrival, under the direction of the FDA, the Company suspended all manufacturing operations in September 2009. o After Caraco voluntarily entered into a consent decree with the FDA, I and my colleagues diligently worked to achieve ...
- 2016 Oct 16
Farmington, MI, 48334
... Improved and maintained an effective quality system that ensured 100 percent compliance to ISO9001 or FDA cGMP respectively. The exposure to different quality systems made me a master of deploying highly effective systems without red-tape. ...
- 2016 Sep 09
Westland, MI
... Position created when FDA mandated full pharmaceutical regulations for Tissue Banks. Hired, trained, and managed engineering team in cGMP, Validation, Six Sigma, RCA, DOE and SPC. Validated software and control systems, packaging, shipping ...
- 2016 Aug 31