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Resumes 21 - 30 of 542 |
Philadelphia, PA
... Knowledge of FDA and HIPPA regulations, medical terminology, laboratory testing procedures and equipment. Familiar with GLP and GCP environment. A highly motivated person with strong analytical and organizational skills. A dedicated team player also ...
- Feb 06
Philadelphia, PA
... Comply to all SOP, cGMP, SAP, AND FDA standards. October 2004- March 2018 Animas Corporation of Johnson & Johnson West Chester, PA Served in several employment capacities and have demonstrated Johnson & Johnson Credo values while fulfilling numerous ...
- Feb 05
Perkasie, PA
... • Designed website and FDA-compliant labels for a line of food products, Chiliboss. The website and labels helped them gain distribution with major retailers. PROFILE Graphic Designer and Illustrator / 1996 - Present Partner and Designer ...
- Jan 29
East Norriton, PA
... Analyst Practice TheraCom, Rockville, MD (client engagement) May 2009 to August 2009 Engaged to perform a Gap Analysis of the current situation within the Software Development Group and define what is needed to create FDA approved software systems. ...
- Jan 27
Ambler, PA
... Scientist/Group Leader 12/2003 to 12/2008 Par Pharmaceutical Companies, Inc (Kali Labs) Spring Valley, NY Executed CMC section for ANDA projects from initial stage of development to final FDA approval with one direct report and two to three on an ...
- Jan 21
Chalfont, PA
... Management, Validation and FDA Compliance, Leading High Performance Teams, CTFA Cleaning/Sanitizing validation, P&G Auditor training, cGMP seminar, PMI (project management Institute) and Lean manufacturing seminars, 6 Sigma, Veeva Vault seminars. ...
- Jan 19
Horsham, PA
... In compliance with SOPs and Food & Drug Administration (FDA) guidelines, performs venipuncture on donors to begin pheresis process. Make necessary adjustments in order to expedite donation time and ensure product quality and donor safety. Maintains ...
- Jan 19
King of Prussia, PA
... Support onsite maintenance of Quality Management system with internal and external audits (Notified Bodies, FDA, customers) Conduct Quality Reviews on Change Requests, validation protocols, design and development documents. Established the use of ...
- Jan 17
Garnet Valley, PA
... Creator and Chairperson of Committee for Product Development, technical transfer to submission, validation and product launch resulting in optimal communication, accountability, flow, timely submissions and product launch per FDA approval schedule. ...
- Jan 11
Philadelphia, PA
... (1997-1999) AstraZeneca FDA regulation compliance Implement ISO best practices/processes Education Master’s Degree (MA) Columbia University NYC NY Biochemistry/Education Bachelor’s Degree (BA) University of Pennsylvania Philadelphia, PA Biochemistry ...
- Jan 10