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Resume alert |
Resumes 1 - 10 of 287 |
Media, PA
... reports at the end of each shift Ensured proper procedures were used to mitigate against cargo loss Worked close with USDA and FDA representatives Ensured warehouse operations were running in compliance with overall goals U.S Army June 2009 - April ...
- Apr 25
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
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
Avondale, PA
... Perform preventive maintenance and repairs to HVAC systems, Adhere to all standards for entering and working in clean rooms while abiding by FDA standards and OSHA guidelines. Perform weekly PMs on the fire system and substations and monthly ...
- Mar 11
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
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
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
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
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
Havertown, PA
... ability to talk with individuals at all levels • Very knowledgeable with CRO, Clinical trial processes, HIPAA and other myriad FDA regulations and compliances Professional Experience Diagnostic Solutions Laboratory 2013-2022 Director, New Business ...
- Feb 22