| Job alert | Jobs 81 - 90 of 1192 |
Associate Scientist I
Inotiv
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Rockville, MD
... Ensure compliance is maintained, continuing Inotiv’s phenomenal track record of successful FDA audits. Assist with ... of bioanalytical experience in the pharmaceutical industry, biotech field or a drug discovery & development or clinical CRO. ... - May 07
QC Associate II - Environmental Monitoring
Charles River Laboratories
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Hungerford Towne, MD, 20850
... the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. ... We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity ... - May 23
Data Modeler
REI Systems
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Sterling, VA
... Clearance: FDA Public Trust clearance must be obtainable Location: Hybrid - locals to DMV area highly preferred. EEO Statement: REI Systems is an Equal Opportunity Employer (Minority/Female/Disability/Vet) - May 12
Quality Manager
Resonetics
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Loudoun County, VA
... The Quality Manager position uses Quality Engineering techniques including: Problem solving using Lean Six Sigma methodology, Process Validations, Process Development and optimization, Gage R&R, reducing dependence on inspection, and ISO compliance. ... - May 09
Supplier Quality Regional Lead
Catalent Pharma Solutions
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Manassas, VA, 20110
... working in an auditing role within the Pharmaceutical/Medical Device industry Knowledge and understanding of the following principles and guidelines: EU EudraLex Volume 4 GMPs, 21 CFR Parts 111/210/211 (FDA), ISO, and related International ... - May 23
QC Scientist
Ryco Biosolutions
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Gaithersburg, MD
... standards and current expectations Established knowledge and application of cGMPs/GLPs, ICH, FDA CMC Guidance Documents Experience with CMC technical sections of regulatory submissions and addressing regulatory authorities on technical matters - May 21
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
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
Logistics Project Manager
BryceTech
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Washington, DC
... closely with logistical support agencies to identify logistical needs and develop plans when product reaches FDA approval. ... Leading and managing a range of clinical and pharmaceutical projects. Strong proficiency in Microsoft Office applications, ... - May 21
Embedded Incident Response Coordination Specialist
Sibylline Americas
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Arlington, VA
... or in other time zones Preferred Qualifications: Bachelor’s degree 2+ years of experience as a leader (supervisory) Lean/Six Sigma experience Experience in emergency management including preparedness and response Experience developing and leading ... - May 21