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Pharm Tech-Certified, Pharmacy, Evenings, Part Time','Part-time','Professional Clinical/Allied Health','2','2','32','32','Occasional','Occasional','KENTUCKY-LOUISVILLE-JEWISH HOSP 200 ABRAHAM FLEXNER','','!*!Responsible for centralized compounding work using safe IV room practices, large volume end-product batching (IVPB, syringes, etc.), compounding total parenteral ..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..
... position reports to the Engineering Validation Sr. Manager and is responsible ... process equipment and facilities CIP/SIP Re-Validation Program and CIP/SIP qualification project ... This position performs process equipment..
Hampton University has established an internal laboratory facility with a workflow that offers PCR-based SARS-CoV-2 assessments for the university community as well as several universities in the Commonwealth of Virginia and ..
... Director, Head of Global Process Validation and is responsible for multi-modality ... is responsible for multi-modality process validation activities in a cGMP environment.u00A0 ... will coordinate and manage process..
... responsible for supporting the method validation program and coordinating and implementing ... management, and method development, optimization, validation and/or troubleshooting. u00A0CHARACTERISTICSu00A0The candidate must ... fully supporting reasoning for conclusions.u00A0u00A0RESPONSIBILITIESu00A0u00A0Define..
TECHNICAL SERVICES SCIENTIST IIJob Summary:This position is viewed as a technical resource in process development and/or daily commercial support. A Technical Services Scientist understands and applies technical principles, theories, and concepts ..
Who We Are It takes a village, and at BioMarin our corporate groups are the people behind our success. Groups such as IT, Finance, Legal, Global Compliance & Ethics, and our ..
We are seeking a QC Scientist I for a very important client. What will you do? Manage service and maintenance of all QC-owned equipment Schedule all service for equipment, coordinating with ..
... Manager of Global MSAT Process Validation and is responsible for multi-modality ... is responsible for multi-modality process validation activities in a cGMP environment. ... will coordinate and manage process..
Why Patients Need YouWhether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients ..