| Resume alert | Resumes 1 - 10 of 306 |
Project Management Application Development
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
... 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
Supply Chain Business Analyst
Frenchtown, NJ
... Common Technical Documents (eCTD) submissions for submitting applications, amendments, supplements, and reports to FDA's Center for Drug Evaluation and Research, Activity & Support Diagrams, validation and testing of clinical trial systems ... - Apr 09
... Common Technical Documents (eCTD) submissions for submitting applications, amendments, supplements, and reports to FDA's Center for Drug Evaluation and Research, Activity & Support Diagrams, validation and testing of clinical trial systems ... - Apr 09
Front Desk Office Assistant
Bethlehem, PA
... • Food Service • Food Handling • Culinary Experience • Food Preparation • Retail Sales • POS • Merchandising • Warehouse distribution • warehouse associate • Baking • FDA regulations • Basic knife skills • Dock worker (1 year) • Warehouse worker (1 ... - Apr 08
... • Food Service • Food Handling • Culinary Experience • Food Preparation • Retail Sales • POS • Merchandising • Warehouse distribution • warehouse associate • Baking • FDA regulations • Basic knife skills • Dock worker (1 year) • Warehouse worker (1 ... - Apr 08
Machine Operator Warehouse Associate
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
... 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
Six Sigma Black Belt
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
... 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
Analytical Development Molecular Biology
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
... • 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
Product Management Market Development
Hellertown, PA
... with researches from academic institutions conducting clinical trials targeted to expand and promote legally cleared FDA clinical claims Supported the International cooperative group “Colon Tumor NBI Interest Group” (CTNIG) in the development ... - Mar 15
... with researches from academic institutions conducting clinical trials targeted to expand and promote legally cleared FDA clinical claims Supported the International cooperative group “Colon Tumor NBI Interest Group” (CTNIG) in the development ... - Mar 15
Pharmaceutical SME RE: PV., Clinical research, Medical monitoring
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
... 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
R D Analytical Chemist
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
... • 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
Business Analyst Quality
Chester Springs, PA
... ●Created all required validation documentation processes as per the guidelines of the FDA. ●Involved in the process of document binder creation which is helpful for the FDA Audit. ●Involved in creating an FDS document for the ARCOS Quarterly report ... - Mar 01
... ●Created all required validation documentation processes as per the guidelines of the FDA. ●Involved in the process of document binder creation which is helpful for the FDA Audit. ●Involved in creating an FDS document for the ARCOS Quarterly report ... - Mar 01