- Charles River Laboratories (Wayne, PA)
- …strongly preferred. + Experience: Minimum 7 year's relevant experience within a contract research, academic or pharmaceutical industry, including experience in ... analysis of biotherapeutics. + An equivalent combination of education and experience with contract research or the pharmaceutical industry may be accepted as a… more
- Contract Pharmacal Corp (Hauppauge, NY)
- …of USP and FDA requirements. + Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products. + Generate method ... validation protocols. + Execute methods validation and...and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities. + Conduct… more
- US Tech Solutions (New Albany, OH)
- **Duration: 12 Month Contract ** **Description:** + The Engineer position reports to the Manager of Engineering under the Engineering & Maintenance team at the Client ... non-routine projects involving the planning, design, reconfiguration, construction, maintenance, validation and alteration of systems, facilities and processes. This… more
- Lilly (Indianapolis, IN)
- …or related experience **Additional Preferences:** + Understanding of medical device and/or pharmaceutical validation + Demonstrated high degree of ownership / ... team (JPT) meetings + Manage commercial tooling and related project work at contract manufacturers + Provide technical injection molding guidance for validation … more
- Charles River Laboratories (Shrewsbury, MA)
- …responsibilities include serving as a Principal Investigator for the development and validation of biomarker, PK and ADA assays (eg: ligand binding assays, enzymatic ... This individual would be responsible for the composition and execution of validation and sample analysis protocols/plan in accordance with company standard operating… more
- Cardinal Health (Indianapolis, IN)
- …for leading the technology transfer activities of clinical phase radiopharmaceuticals under contract with innovator partners. + As a member of the technical ... selection, process and analytical equipment configuration, document creation, method validation , and process qualification, as well as occasional production and… more
- Gilead Sciences, Inc. (Foster City, CA)
- … pharmaceutical ICH guidance + Solid understanding of the contract manufacturing organization (CMO) landscape; knowledge of CMO capabilities and limitations ... through execution of manufacturing campaigns within our global external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements,… more
- Astellas Pharma (Westborough, MA)
- …as at contract labs and CMOs. + Support QC equipment validation , maintenance, calibration, and QC laboratories scheduling and maintenance. + Participate and own ... you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries...manufacturing samples for QC analysis, ship samples to the contract labs testing, review data for lot disposition. +… more
- Cambrex High Point (Charles City, IA)
- …may be assigned. Qualifications/Skills + Strong knowledge of GMP regulations, validation practices, and pharmaceutical production processes. + Proficient in ... Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …experience in a high-volume pharmaceutical manufacturing QC laboratory or contract pharmaceutical analytical laboratory testing organization is a plus. + ... Scientist I conducts routine and non-routine analyses of raw materials, validation , and stability samples by appropriate analytical methods. The Senior Scientist… more
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