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Resumes 41 - 50 of 154 |
Hatfield, PA, 19440
... Carries a proven track record of success in identifying and implementing operational cost savings and productivity improvements while maintaining adherence to strict regulatory standards for FDA and ISO. Excels in directing and leading teams in ...
- 2018 Jun 27
Bethlehem, PA
... of Clarion, Clarion, PA (Double Major: Biology and Physical Science) (Recruited College Wrestler) PROFESSIONAL DEVELOPMENT FDA Compliance Training 21 CFR Training Program (CSSC Inc.) Lean / Sigma Workshop (ASQ) Green Belt Certification – Lean-Six ...
- 2018 May 21
Washington, NJ, 07882
... Developed and Instituted FDA protocols, IQ’s, OQ’s, and PQ’s for various process and packaging machinery. Developed a Training Program with PMMI to improve our overall staff of employees, in the areas of,Mechanical,Pneumatic, Hydraulic, Basic ...
- 2018 Apr 10
Emmaus, PA, 18049
... responsible for all aspects of infrastructure including but not limited to Staffing, Sales, Training, FDA Testing, Sourcing and Procurement. Sr. Account Consultant- GMC D&B, 2003-Nov 2004 Supported $7M in contract revenue through relationship ...
- 2018 Mar 23
Sellersville, PA, 18960
... EDI Testing Web Testing Performance Volume testing Data Mining Sarbanes-Oxley Act (SOX), Clinical Practice/CFR Part 11 FDA regulatory (Drug management) TECHNICAL SKILLS: Operating Systems: MVS, Windows NT/2000 4.0/XP, UNIX, AS/400 RDBMS: Oracle ...
- 2018 Feb 01
Easton, PA
... As of date, I am very familiar with G.M.P's, S.O.P's and ISO and work with FDA regulated and non FDA products. I am applying for a compounder/batch maker with your company. Please take a moment to review my qualifications and resume. You'll see that ...
- 2018 Jan 16
Bethlehem, PA
... TRAINING: Computers, T.Q.M, S.P.C, T.P.M, Six Sigma, Team Building, Self-directed Work teams, M.R.P, E.R.P & SAP, OSHA & GMP regulations, USDA, FDA, HACCP, CIP, NSF, SQF Practitioner, Safety Committees and Pepsi CQV process. SALARY: Open.
- 2018 Jan 12
Easton, PA, 18042
... Member of the site Quality Leadership Team (QLT) Additional Responsibilities and Laboratory Experience Trained on all applicable ISO 9001, FDA, and current Good Manufacturing Practices (cGMPs) as they pertain to the industrial gases industry Proven ...
- 2017 Oct 07
Phillipsburg, NJ, 08865
... ahead of any areas of potential problems Supervisor 2004 - 2006 Maintained proper documentation in accordance with: DDD, FDA, GDP Responsible for regulating cold storage of vials and controlled medication counts: Calcitonin, Phenobarbital, Lyrica ...
- 2017 Aug 05
Slatington, PA
... FDA). Technical writing experience related to investigations into manufacturing process variation. Complete batch record documentation accurately and all appropriate log books and cGMP related documentation as necessary. While practicing consistent ...
- 2017 Jul 31