|
Resume alert |
Resumes 71 - 80 of 80 |
Easton, PA, 18042
... Proficiently filled prescriptions for hospital patients in compliance with FDA and internal standards . Managed restocking and pre-packaging of generic medication as well as replaced all medications in Pyxis machine; verified inventory use for ...
- 2010 Oct 06
Forks, PA
... (TCO) • Analyzed return on investment (ROI) • Labware LIMS implementation lead • SQLLIMS technical lead • Lead team to respond to FDA audit finding • SME to TotalChrom • Waters Empower implementation • Created corporate Crystal Reports • Corporate ...
- 2010 Sep 20
Easton, PA, 18045
... Review incoming inspection data a custom parts and resolve quality problems to insure GMP and FDA compliance. Responsible for a number of multi-million dollar projects which included engineering, designing, purchasing parts, fabricating, testing and ...
- 2010 Sep 13
Bethlehem, PA, 18020
... Attended meetings with SOP authors to discus technical, compliance and formatting issues 2000 -2001: Compliance Coordination Auditor (through Joule Scientific) ( Reviewed analytical data for FDA submission ( Wrote audit reports ( Reviewed company ...
- 2010 Aug 10
Lehigh Valley, PA, 18002
... Strong integration of technical knowledge and skills to deliver superior management outcomes including significant experience in operations, engineering, EHS, maintenance, QA/QC, technical programs, automation and FDA audit readiness. CORE ...
- 2010 Aug 03
Easton, PA, 18040
... Upgrade and develop Quality systems to comply with AS9100, FDA 21 CFR Part 820 and ISO 13845 requirements . Improve supplier and internal team performance, training on latest Six Sigma, Lean Engineering, PPAP, CAPA and PFMEA ( risk mitigation tool) ...
- 2010 Jul 22
Kunkletown, PA, 18058
... Product Sales, Marketing and Development, Inventory Control, Union and Management Training, Vendor Relationships, Team Builder, Interpersonal Skills, Manufacturing Management and NJDEP / EPA / FDA / OSHA and Other Regulatory Compliance. ...
- 2010 Jul 13
Easton, PA, 18045
... In depth knowledge of regulatory requirements, including, cGMPs, GLPs, GCPs, QSRs, FDA, EMEA, & CMDR regulations, ICH guidelines and ISO guidelines 9001, 13845, 14000, 14971. . Adept a data mining, extracting information and reducing data complexity ...
- 2010 Jun 07
Easton, PA, 18045
... Strong understanding of FDA regulations, 21 CFR Part 11, ICH and GCP guidelines and other Regulatory Submissions. . Good interpersonal skills; excellent organizational skills, capable of handling multiple tasks and priorities and ability to interact ...
- 2010 Jun 01
Saylorsburg, PA, 18353
... Ciba-Geigy Corporation (now NOVARTIS) 1989-1994 Research Scientist, Research Department, responsible for process development, generating and validation and auditing of protocols, data and formulations under DEA and FDA cGMP/cGLP regulations. ...
- 2010 Mar 09