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Downingtown, PA
... Acquired proficiency in Pharma validation Projects (GxP, GMP, CFR 11 & FDA) Facilitated Release tracking and Release Management cycles internal and integration. Rama Markapuram, PMP® LinkedIn TOSCA - Specialist 2 Scrum Master - Internal ...
- May 22
Wilmington, DE
... Administrator Assistant GlaxoSmithKline March 2002 to August 2004 Assist Quality Engineers with Notice of Events Investigations Assist Training Manager with entering, documenting and filing employee's GMP training records. Assist with coordinating ...
- May 02
Exton, PA, 19341
... ● Applied and implemented Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs) to clinical supplies inventory and warehousing workflow. ● Distributed finished clinical supplies to clinical study research sites throughout the ...
- Apr 04
Wilmington, DE
... protein expression, purification & activity assay 2 years excellent experience in Pharmaceutical Industry in aseptic technique & GMP/GLP regulation Very good analytical and experimental skills to execute adequately in new projects and meet tight ...
- Mar 26
New Castle, DE
... Has a full understanding of GMP, OSHA, & SHE practices. Areas of expertise include inventory control, shipping, receiving, packing, quality control inspection, invoicing, and data entry. Capable of multi-tasking, communicating efficiently, and ...
- Feb 14
Springfield, PA
... Responsibilities include working in a GMP lab setting, conducting personnel and environmental monitoring for the presence of microbes to assure products remain sterile, counting bacterial colonies from environmental monitoring to determine CFUs, ...
- Feb 05
Avondale, PA
... •Responsible for product quality and development by stablishing traceability, Maintaining the proper level of regulatory compliance, GMP and a comprehensive SOP. •Responsible for all technical related discussion and method development •Works ...
- Feb 04
Swedesboro, NJ
... Proficient in global GMP and Regulatory requirements. Working knowledge in CAPAs, INDs, recalls, QA, JDE, Literature, legal (litigations), clinical trials (drugs: phases I to IV – medical device: class 1-3 – transplantable devices, mesh, minimally ...
- 2023 Dec 08
Swedesboro, NJ
... Strong knowledge of EPA, FDS, GMP, OSHA, DOT, and HAZMAT regulations within ISO 9000 environment. Possess deep understanding of Lean Six Sigma methodologies. Areas of Expertise • Warehouse Operations Management • Continuous Process Improvement • ...
- 2023 Nov 24
Lansdowne, PA
... Promoting the development and implementation of strategic projects assuring compliance with established policies/procedures of the Division and Corporation and complies with all applicable governmental regulations Good Manufacturing Practice (GMP), ...
- 2023 Nov 13