- Sartorius (CA)
- …perspectives. + Practical experience in pilot and production-scale process development . + Strong knowledge of cGMP bioprocessing operations and regulatory ... Sartorius is seeking a driven and collaborative Platform Development Specialist - Gene Therapy to...Minimum 2 years of hands-on experience in gene therapy process development or production. + Deep understanding… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …timely completion of associated operations/documentation, and assisting in the monitoring of cGMP compliance. As a Principal External Manufacturing Specialist , a ... manufacturers or business partners. + Leads a sub-team in continuous process improvements, system/equipment implementation and/or strategy development . +… more
- Unither Pharmaceuticals (Rochester, NY)
- …sampled, packaged, tested, held, and released in a manner consistent with cGMP requirements. The Compliance Specialist effectively conducts and supports problem ... Compliance Specialist I Who we are? We are a...than 300 employees. Your role Reporting to the Quality Development and Compliance Manager, JOB SUMMARY: + The Compliance… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …+ May manage direct reports and/or lead a sub-team in continuous process improvements, system/equipment implementation and/or strategy development . + You have ... Regeneron is currently looking for a Principal External Manufacturing (EM) Specialist to join the Advanced Therapies External Manufacturing Team that specializes in… more
- Takeda Pharmaceuticals (Libertyville, IL)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... the best of my knowledge. **Job Description** **About the Role:** The Learning Specialist , as part of the Site Business Excellence organization, manages the Learning… more
- PACIV (San Juan, PR)
- …its Puerto Rico office. Job Description: The Computerized System Validation (CSV) Specialist /Engineer will be responsible for development and execution of ... Industry, mainly Bio-Pharma and/or Medical Devices. The resource will be responsible for development and execution of CSV deliverables, as per System Development … more
- Kelly Services (Winston Salem, NC)
- …with incoming material qualification testing and lot release evaluations. + Support process development , validation activities, and data collection for ... **Manufacturing Specialist III - Cell Processing** **Location: Winston Salem...processing techniques, procedures, and regulatory compliance. + Drive continuous process improvement, incident investigations, and deviation resolutions. + Ensure… more
- Catalent Pharma Solutions (Manassas, VA)
- **Quality Assurance Specialist I** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... service to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested experience in … more
- Bristol Myers Squibb (Indianapolis, IN)
- …with RayzeBio policies, standards, procedures and global current Good Manufacturing Practice ( cGMP ). The Senior Specialist provides Quality support and oversight ... aims to be the global leader in radiopharmaceuticals. **Summary** The Senior Specialist , QA Operations will help support operations through quality oversight in a… more
- Merck (Wilmington, DE)
- …We invite you to become a part of our journey as the Manufacturing Senior Specialist Drug substance. This role offers you the chance to contribute to the site's ... development and ensure successful GMP manufacturing. In this position the Manufacturing Senior Specialist will play a pivotal role in ensuring smooth operation of… more
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