- JobsRUs (Rocklin, CA)
- …analysis, process improvement, and team collaborationResponsible for Process Development , Manufacturing, Regulatory Affairs, and Project Management ... teams to achieve successful outcomes.Collaborates with key stakeholders such as Process Development , Manufacturing, Regulatory Affairs, and Project Management… more
- University of Southern California (Los Angeles, CA)
- …in the university's current Good Manufacturing Practices ( cGMP ) facility. The Process Development Specialist is responsible for developing procedures and ... Process Development SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - Process - Development - Specialist \_REQ20145450/apply) Keck School… more
- Strata-G, LLC (TN)
- …results of our successes with the community. Strata-G is seeking an experienced cGMP Quality Specialist with the following: Summary: The Quality Representative ... approval for release of radioisotope products for distribution + Assist in the development of technical procedures and documents, and assess for implementation of QA… more
- Stanford University (Stanford, CA)
- …Gene Medicine (LCGM) at Stanford University School of Medicine is seeking a Manufacturing Specialist for the process development and manufacturing team. The ... Manufacturing Specialist **School of Medicine, Stanford, California, United States**...Gene Therapy manufacturing facility that provides regulatory, quality systems, process development and manufacturing support to the… more
- Catalent Pharma Solutions (Harmans, MD)
- …and a warehouse. The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage ... **Sr. Specialist , QA OTF** **Position Summary** Catalent is a...a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- Regeneron is currently looking for an Analytical Development Specialist for our QC Analytical Sciences Bioassay team with a Monday-Friday, 8am-4:30pm schedule. ... The Analytical Development Specialist develops new Quality Control (QC)...standard operating procedures at the qualification, validation, or transfer process . + Applies a fundamental understanding of the science… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …manufacturers or business partners. * Leads a sub-team in continuous process improvements, system/equipment implementation and/or strategy development . * ... We are currently looking to fill an External Manufacturing Specialist position. The External Manufacturing Specialist oversees all aspects of contract… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- …teams. Interfaces with Engineering, Procurement, Quality Control, Quality Assurance, Process Development , Project Managers, Validation and Manufacturing ... **Documentation Specialist , Analytical Research & Development ** **Position...of document change control procedures and philosophies within a cGMP environment. Catalent is committed to a Patient First… more
- Catalent Pharma Solutions (Harmans, MD)
- …and a warehouse. The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage ... **Senior Specialist , QA Analytical** **Position Summary** Catalent is a...client audits/inspections of Catalent. * Provide quality oversight of process and analytical method development in an… more
- ThermoFisher Scientific (Allentown, PA)
- …of global clinical supply chain. With unwavering commitment to service, science and process engineering, we are powered by people with an exceptional commitment to ... they do matters. Discover Impactful Work: The Operations, Clinical Quality Assurance Specialist II will support all Quality functions in relation to packaging… more
- Catalent Pharma Solutions (Manassas, VA)
- **Quality Assurance Specialist I - Quarantine** **Position Summary** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical ... industry in the development and manufacturing of new treatments for patients worldwide....engaging new products consumers will love. The Quality Assurance Specialist I - Quarantine is responsible for auditing the… more
- Astellas Pharma (Westborough, MA)
- **Sr Manufacturing Specialist , Production Planning** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, ... a wholly owned subsidiary of Astellas Pharma Inc and focused on the development and commercialization of stem cell and regenerative medicine therapies. Astellas is… more
- Bristol Myers Squibb (Summit, NJ)
- …better place than here at BMS with our Cell Therapy team. The Principal Specialist Quality Risk Management CAR T is responsible for supporting the S-12 Cell Therapy ... identify risk areas and implement risk mitigation measures for S-12 operations, cGMP compliance and business continuity. Additionally, this role is responsible to… more
- Kelly Services (Louisville, CO)
- **Sr. Quality Assurance Specialist - Louisville, CO** **Type:** Contract (6 months - potential for extension/conversion) **Shift:** M-F 8a-5p **Pay Rate:** ... **Position Summary** We are seeking a Contract Quality Assurance (QA) Sr. Specialist to support deviation investigations related to Good Manufacturing Practice (GMP)… more
- J&J Family of Companies (Raritan, NJ)
- QA Lab Oversight Specialist II - 2406211546W **Description** Johnson & Johnson is recruiting for a QA Lab Oversight Specialist , located in Raritan, NJ! At ... successful transfer of QC Lab functions to the Raritan cGMP facility to test products. + Review and approve...the interpretation of quality issues and participates in the development of technical or scientific initiatives and activities. +… more
- ThermoFisher Scientific (San Francisco, CA)
- …Fisher Scientific's broad portfolio of solutions and clinical and commercial cGMP cell therapy manufacturing services, along with associated technology ... development support to our partners. In the Cell Therapy...for a variety of unmet medical needs. The QA Specialist II will provide Quality oversight for projects, performs… more
- ManpowerGroup (Sellersville, PA)
- …is looking for hardworking, motivated talent to join their team. As a ** Development Testing Specialist ** you will provide **operational support, customer cycle ... and washing. + Assist Management and Staff during the quote process by completing cycle development /performance qualifications questionnaires. + Collect… more
- Hovione (East Windsor, NJ)
- …reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and ... it for life. You will be responsible to: Guarantees cGMP compliance in all activities and systems related to...documents (PdAs) as required and appropriate - Approve IOPs, process master documentation and product specifications as required and… more
- Bausch + Lomb (Tampa, FL)
- …qualify/validate any of the above validation elements following the latest cGMP regulations. 3. Assess and perform timely process /equipment/systems ... over our 170-year history. We have a significant global research, development , manufacturing, and commercial footprint of approximately 13,000 employees and a… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- **Summary:** The External Manufacturing Principal Specialist provides technical and process support for all aspects of clinical and commercial parenteral drug ... specific work instructions and SOP's. + Lead sub-team in continuous process improvements, system/equipment implementation and/or strategy development . + Support… more
