- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the full ... - Required Experience and Skills: Minimum of five (5) years of manufacturing , technology, laboratory, and/or quality operations experience within GMP environment GMP… more
- Fujifilm (Holly Springs, NC)
- …a 2-2-3 calendar rotation. Please note that this posting** **represents** ** multiple ** **openings within our manufacturing organization **Company Overview** ... or GED with 2 years of related experience in Life Sciences Manufacturing **OR** + Associate 's Degree in Life Sciences with 0 years of related experience **OR**… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- … Quality Assurance support, including oversight of upstream and downstream biologics manufacturing processes, ensuring compliance with biologics -specific ... **Job Summary** The Associate Director, Global Product Quality - Biologics...commercial products and/or development projects. + Proven experience with biologics GMP manufacturing , including upstream (cell culture,… more
- United Therapeutics (Research Triangle Park, NC)
- …GxP events + Interact regularly with peers and senior management across multiple functional groups (eg, Research and Development, Manufacturing , Validation, ... expertise and mentoring or developing a member of your team. The Associate Director, QA Engineering will provide advanced support and subject matter technical… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …Thursday/Monday - Friday** Due to the growth at the GT site and ramping up multiple Manufacturing departments, it is vital that we focus on training newer ... existing area expertise while we work through this growth phase, no GT Manufacturing production employees are eligible to bid for this position at this time.… more
- Merck (Durham, NC)
- **Job Description** The Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the ... Experience and Skills:** + Minimum of five (5) years of manufacturing , technology, laboratory, and/or quality operations experience within GMP environment +… more
