| Resume alert | Resumes 1 - 10 of 287 |
Project Manager Drug Development
Blue Bell, PA, 19422
... Assessed mechanism of action for a $40M in-licensed compound for psoriasis, FDA-approved. Evaluated an anti-sense oligonucleotide for cytoprotection; data was part of a patent and a publication. Organized biology efforts and worked as co-lead author ... - May 03
... Assessed mechanism of action for a $40M in-licensed compound for psoriasis, FDA-approved. Evaluated an anti-sense oligonucleotide for cytoprotection; data was part of a patent and a publication. Organized biology efforts and worked as co-lead author ... - May 03
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
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
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
Supply Chain Master Control
Coatesville, PA
... where needed Report to Executive Management / Field / Internal Team – updates / department goals achieved On-going training for FDA/PMA regulations as needed Weekly Back Order Report and Fulfillment Schedules – Assess and utilize 03/2020 – 09/2021; ... - Mar 07
... where needed Report to Executive Management / Field / Internal Team – updates / department goals achieved On-going training for FDA/PMA regulations as needed Weekly Back Order Report and Fulfillment Schedules – Assess and utilize 03/2020 – 09/2021; ... - Mar 07
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
Design Engineer Product Development
West Chester, PA
... Experience within a regulated industry (medical devices desirable, along with knowledge of Product Lifecycle Management, FDA Quality System Regulations and ISO 13485) Responsible for tracking of CR/CN in Windchill with Approval from stakeholders ... - Mar 04
... Experience within a regulated industry (medical devices desirable, along with knowledge of Product Lifecycle Management, FDA Quality System Regulations and ISO 13485) Responsible for tracking of CR/CN in Windchill with Approval from stakeholders ... - Mar 04
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