| Resume alert | Resumes 61 - 70 of 78 |
Manager Training
Andover, NJ
... Comply with FDA and DEA regulations both Importing and Exporting. Training, Retraining, Coaching and Counseling a staff of 46 Union and Non Union employees. Training in DOT 49 CFR Detailed Function Specific Training, DPCC (Discharge Prevention ... - 2012 Jul 29
... Comply with FDA and DEA regulations both Importing and Exporting. Training, Retraining, Coaching and Counseling a staff of 46 Union and Non Union employees. Training in DOT 49 CFR Detailed Function Specific Training, DPCC (Discharge Prevention ... - 2012 Jul 29
Quality Assurance Control
Stewartsville, NJ, 08886
Experienced Pharmaceutical scientist with expertise in the GMP compliant handling and submission of samples submitted for Quality Control testing according to FDA, EU and JP testing requirements. Performs trending, tracking of testing records and ... - 2012 Jun 03
Experienced Pharmaceutical scientist with expertise in the GMP compliant handling and submission of samples submitted for Quality Control testing according to FDA, EU and JP testing requirements. Performs trending, tracking of testing records and ... - 2012 Jun 03
Safety Manager
Port Murray, NJ
... medical review of incoming SAE reports (Individual Case Reviews: review and approval of all potential expedited reports), working with Regulatory Affairs to determine reporting timelines, and assist with the submission of safety reports to the FDA. ... - 2012 Mar 29
... medical review of incoming SAE reports (Individual Case Reviews: review and approval of all potential expedited reports), working with Regulatory Affairs to determine reporting timelines, and assist with the submission of safety reports to the FDA. ... - 2012 Mar 29
Data Management
East Stroudsburg, PA, 18302
... Senior Data Technician •Accurately entered verbal and numerical data from clinical trials into computer programs for statistical analysis in preparation for FDA submission. •Generated verification reports and made the necessary corrections to study ... - 2011 Aug 24
... Senior Data Technician •Accurately entered verbal and numerical data from clinical trials into computer programs for statistical analysis in preparation for FDA submission. •Generated verification reports and made the necessary corrections to study ... - 2011 Aug 24
Management Data
Stroudsburg, PA, 18360
... This Charter was submitted to the FDA and approved on first submission. Managed and led a team of nine Clinical Data Managers and Clinical Data Analysts. Global Lead Data Manager on second pivotal trial being run via the UK office. My participation ... - 2011 May 10
... This Charter was submitted to the FDA and approved on first submission. Managed and led a team of nine Clinical Data Managers and Clinical Data Analysts. Global Lead Data Manager on second pivotal trial being run via the UK office. My participation ... - 2011 May 10
Project Manager Quality Assurance
Hackettstown, NJ, 07840
... Excellent knowledge of GLPs and FDA submission process. Impressive people skills and ability to communicate complex ideas to management. Talent for structuring and implementing programs/policies that drive the business forward. EDUCATION: PhD ... - 2011 Feb 22
... Excellent knowledge of GLPs and FDA submission process. Impressive people skills and ability to communicate complex ideas to management. Talent for structuring and implementing programs/policies that drive the business forward. EDUCATION: PhD ... - 2011 Feb 22
Administrative Assistant Manager
Easton, PA, 18040
... Logged, tracked, and trended FDA filings within a dedicated database in an effort to enhance a results-oriented business compliance program in accordance with legal and regulatory requirements. . Utilization of strong organizational, analytical, and ... - 2011 Jan 24
... Logged, tracked, and trended FDA filings within a dedicated database in an effort to enhance a results-oriented business compliance program in accordance with legal and regulatory requirements. . Utilization of strong organizational, analytical, and ... - 2011 Jan 24
Quality Assurance Engineer
East Stroudsburg, PA, 18302
... Diverse state-of-the-art manufacturing background in electronics, microwave, plastics, and heavy industries governed by ISO, GMP, FDA and military quality system requirements. Skilled in developing and managing domestic and international suppliers. ... - 2010 Nov 01
... Diverse state-of-the-art manufacturing background in electronics, microwave, plastics, and heavy industries governed by ISO, GMP, FDA and military quality system requirements. Skilled in developing and managing domestic and international suppliers. ... - 2010 Nov 01
Quality Assurance Product Development
Easton, PA, 18042
... Control Ergonomic Design ISO 9001 GMP's (Good Manufacturing Practices) Master Control FDA Complaint ECN (Engineering Change Notice), Design Control, CAR (Corrective Action Request) FDA Inspection Hazard Communication QSR (Quality System Regulation) - 2010 Oct 29
... Control Ergonomic Design ISO 9001 GMP's (Good Manufacturing Practices) Master Control FDA Complaint ECN (Engineering Change Notice), Design Control, CAR (Corrective Action Request) FDA Inspection Hazard Communication QSR (Quality System Regulation) - 2010 Oct 29
Customer Service Sales
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
... 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