|
Resume alert |
Resumes 1 - 10 of 586 |
Lansdale, PA
... Project 6: ClinPharm and CTS (Clinical Trial Suite) Application Upgrade, Support, and Retirement from 2009 – 2019 Description: CTS reduced the cycle time of clinical trials and regulatory (FDA) submissions to improve the accuracy and efficiency of ...
- Apr 14
Philadelphia, PA
... • Ensure compliance to SOPs, and FDA regulations. • Participate in PINAL inspections as well as Other health authorities as a subject expert. • Ensure that materials are delivered to appropriate areas, monitor flow of goods and verify incoming ...
- Apr 10
Norristown, PA
... with 8 years of experience with Rotoflex/Karlville slitting and rewind machine ● Trained on and comply with GMP, OSHA, and FDA regulations ● Dedicated employee with strong interpersonal and problem-solving skills ● Flexible team player who adapts ...
- Mar 28
Philadelphia, PA
... Strong knowledge of USP/EP, ICH and FDA requirements for drug applications. Excellent communication skills, project leadership, ability to coach and develop direct reports. WORK EXPERIENCE AAA PHARMACEUTICAL INC., Lumberton, NJ 2015-2020 Quality ...
- Mar 28
Philadelphia, PA
... training certificate in Catering and Restaurant Management Graduated in May, 2014 ● Customer Service ● Catering ● Banquet Serving and Organization ● Galley Work ● Serving and Food Expo, FDA Certified ● Hotel Administration ● Food Prep ● Housekeeping
- Mar 26
Ambler, PA
... by 75% ABBOTT LABORATORIES Global Director of Lean Six Sigma 2003 - 2005 • Implemented a world-class Business Excellence program (DMAIC, Lean Manufacturing, and DFSS) into Abbott Diagnostic’s business within the confines of GMP and FDA oversight. ...
- Mar 26
Havertown, PA, 19083
... SOPs Streamlined continuous improvement processes and program management which generated improved KPIs, financial metrics Met FDA deadlines for Alkermes safety updates by working closely with internal Medical Legal Review process Team Lead Vaccine ...
- Mar 26
Lansdale, PA, 19446
... • Conducted assessment of the IND/BLA filings in compliance with FDA regulatory and pharmacopeial guidelines. • Supervised and trained technical staff. Shin-Yi Du, Ph. D., Resume – Page 1/2 P A G Postdoctoral Fellow (2019 – 2021) Northwell Health - ...
- Mar 24
Schwenksville, PA
... Jul-2012 – Jul-2014 Adverse Experience Reporting Coordinator III (contract position) ·Determines, on the basis of SOP’s and FDA regulations, the prompt or periodic classification of each adverse experience contained in the reports received for Merck ...
- Mar 09
Malvern, PA
... • Reviewed lab personnel notebooks for compliance with FDA regulations and internal SOPs. • Recipient of an Above & Beyond Award. EDUCATION MS, Biochemistry, East China University of Science and Technology, Shanghai, China Thesis: Chemical ...
- Mar 05