- Fujifilm (College Station, TX)
- …product related activities; Assisting with Quality audit functions; Identifying process and Quality System improvements. **Reports to** Supervisor/Manager, QA **Work ... final product containers and review and/or approval of executed process records and data. + Assist in Quality audits...Audit of equipment logbooks + Review of vendor, supplier, contract laboratory audit questionnaires + Notify Senior Management of… more
- Catalent Pharma Solutions (Greenville, NC)
- …performed by Packaging Line Operators. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... is completed with minimal errors. + Perform start-up and in- process testing accurately and ensure proper documentation Complete QAD...degree with 2 years of relevant experience in the pharmaceutical industry or; + Associate degree with 5 years… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and propose innovative solutions to accelerate the development and approval process , leveraging the full breadth of regulatory pathways. The incumbent will ... in the assigned therapeutic area from the global regulatory, scientific, pharmaceutical , pharmacovigilance, market access and commercial perspective as well as… more
- Cambrex High Point (High Point, NC)
- Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug ... toward key synthetic intermediates and APIs. Experimental skills related to chemical process development and kilo - scale synthesis of organic compounds of medicinal… more
- Otsuka America Pharmaceutical Inc. (Rockville, MD)
- …integrate new technical capabilities into the end-to-end clinical development process and associated platforms/eco-systems. Ensure solutions being planned, take ... Project or Technical Management, Change Management methodology, financial/budget and contract management. **Compensation:** $200,000 - $225,000 annually + benefits… more
- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- …based on clinical protocols + Serve as primary point of contact for contract packaging, distribution, and storage vendors + Prepare clinical packaging timelines and ... in Life Sciences, Pharmacy or related scientific discipline + 3 years pharmaceutical industry experience + Some knowledge of GMPs (current Good Manufacturing… more
- Dr. Reddy's Laboratories (Princeton, NJ)
- …Laboratory and Manufacturing investigations, Product Specifications, Analytical Method Validation, Process Validation, Method and process Transfer and major ... on monitoring of trend data. + Reviews Analytical method and process development, enhancements and validation/verification, transfer related documents and raw data… more
- Otsuka America Pharmaceutical Inc. (Helena, MT)
- …initiatives to enhance sales force productivity through system automation and process efficiencies. **Field Support & Adoption** + Serve as a liaison ... reliability and ongoing enhancements. + Contribute to vendor selection, contract negotiations, and service-level agreements. **Qualifications & Experience** **Required:**… more
- Fujifilm (College Station, TX)
- …related activities; Assisting in and performing Quality audit functions; Identifying process and Quality System improvements; Acting as a QA liaison internally. ... logbooks + Act as a QA liaison to internal Departments and Vendor/ Contract Laboratory Quality Groups. + Notify Supervisor of potential quality or regulatory… more
- Curia (Albuquerque, NM)
- …operation, providing technical support for validated systems. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ... experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to...and execute required protocols and complete reports for equipment, process utility, test, and revalidations as assigned. + Develop… more