- SOFIE (Totowa, NJ)
- Help shape the future of nuclear medicine! SOFIE is seeking a Product Development Specialist to lead the development , implementation, and validation of ... we want to hear from you. Title | Product Development Specialist Location | Totowa, NJ Department...and maintenance instructions, and procedure manuals required. Knowledge of cGMP requirements, aseptic process (cleanroom environment), and… more
- Genentech (San Francisco, CA)
- …own the strategy and execution across three core pillars: Data Governance & Process : Oversee and manage a robust data governance framework for 30,000+ assets, ... Given the highly regulated environment, ensure services comply with OSHA, cGMP , environmental, and other regulations. Collaborate across global teams to support… more
- Kelly Services (Irvine, CA)
- **Job Title:** QA Validation Specialist (Contract) **Duration:** 10 months **Location:** Irvine, CA (onsite) **Rate:** $38-40/hr. This position involves hands-on ... in regulated environments and enjoy driving projects from protocol development through audit-ready execution. **RESPONSIBILITIES:** + Assists in assuring facility,… 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
- Bristol Myers Squibb (Bothell, WA)
- …lives. Read more: careers.bms.com/working-with-us . The primary focus of the Senior Specialist - MSAT Cell Therapy Engineering Services, Process Support is ... Myers Squibb's GMP facility in Bothell, WA. The Senior Specialist - MSAT Cell Therapy Engineering Services, Process...relevant experience in biologics or cell therapy manufacturing or development with BS, or 2+ years relevant experience with… 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
- Catalent Pharma Solutions (Princeton, NJ)
- …the dedicated Client QA Representative, partnering with cross-functional teams-Manufacturing, Process Development , Technology Transfer, and more-to maintain site ... **Senior Specialist , Quality Operations** **Position Summary:** + **Work Schedule:...by pharma, biotech and self-care companies to accelerate the development , manufacturing and delivery of products that improve lives.… more
- Herbalife (Lake Forest, CA)
- …that ensures each teammate gains a holistic understanding of the development process through commercialization. **Qualifications** SKILLS AND BACKGROUND REQUIRED ... Specialist , Document (Technical Operations) Category: Manufacturing Position Type:...to ensure manufacturing batch records encompass all compliance and process requirements. **HOW YOU WOULD CONTRIBUTE:** + Prepare and… more
- Bristol Myers Squibb (Manati, PR)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Specialist , Process Automation will support the Manati site's manufacturing, ... problems. + Attends to all mandatory training meetings for cGMP 's, EHS and Company Policies. + Performs process...be directed to Chat with Ripley. R1598065 : Senior Specialist , Process Automation **Company:** Bristol-Myers Squibb **Req… 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 ... to be the global leader in radiopharmaceuticals. **Summary** The Senior Specialist , External Manufacturing Quality Assurance is responsible for quality oversight of… more
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