| Job alert | Jobs 71 - 80 of 1193 |
Principal Scientist, AR&D
Granules
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Chantilly, VA, 20151
... Draft the analytical method validation protocols and reports Performs testing of pharmaceutical raw materials, bulk and ... Maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. Maintain laboratory notebooks ... - May 11
Production Operator I - III (Solid Dosage/OSD Manufacturing)
Granules
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Chantilly, VA, 20151
... Key Accountabilities: Operates pharmaceutical production machinery and follows the procedures for manufacturing such as ... Knowledgeable of FDA regulations, GMP, Lean Manufacturing, Six-Sigma, etc. Solid working knowledge and skills in procedures, ... - May 01
Warehouse Coordinator (Temp to perm)
Granules
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Bull Run, VA, 20109
... 1-2 years’ experience in pharmaceutical/food industry. Manufacturing: 2 years (Preferred) cGMP environment: 2 years (Preferred) FDA and OSHA regulations: 2 years (Preferred) - May 02
Clinical Advisor
Axle
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Rockville, MD
... Ensure that pharmaceutical concerns raised during the DCRC and other meetings are addressed in a timely manner. Advise the protocol team regarding pharmaceutical issues relating to DAIT/NIAID standards, FDA and other Health Authorities regulations, ... - May 09
Clinical Advisor
Axle
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Rockville, MD
... Ensure that pharmaceutical concerns raised during the DCRC and other meetings are addressed in a timely manner. Advise the protocol team regarding pharmaceutical issues relating to DAIT/NIAID standards, FDA and other Health Authorities regulations, ... - May 09
Packaging Operator/Materials Handler (1st & 2nd Shifts )
Granules
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Bull Run, VA, 20109
... product, and raw material management (bottles, caps, cartons), on our oral solid dosage pharmaceutical packaging line. ... Follow Current Good Manufacturing Practices (cGMP) Food and Drug Administration (FDA) and other regulatory requirements. ... - May 05
Project Manager 3
Charles River Laboratories
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Poolesville, MD, 20837
... Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and ... We have proudly supported the development of >80% of the drugs approved by the FDA for the past 3 years. Equal Employment ... - Apr 12
FDA - Deputy Division Director Division of Clinical Evidence and
AE Strategies
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Silver Spring, MD
... Cures SOD – OCEA/DCEA3 Deputy Division Director The Deputy Director supports the the DCEA3 Director in efforts to direct and measure the effects and quality of all aspects of activities under FDA’s national Medical Product Safety Network, MedSun, ... - Apr 28
Medical Officer
Axle
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Rockville, MD
... Provide clinical and scientific information for preparing NIAID communications to the Food and Drug Administration (FDA), other government and nongovernmental agencies, pharmaceutical companies and Data Safety Monitoring Boards. Conducts site visits ... - May 09
Medical Officer
Axle
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Rockville, MD
... Provide clinical and scientific information for preparing NIAID communications to the Food and Drug Administration (FDA), other government and nongovernmental agencies, pharmaceutical companies and Data Safety Monitoring Boards. Conducts site visits ... - May 09