- Lilly (Durham, NC)
- …detail-oriented Visual Inspection Subject Matter Expert (SME) specializing in parenteral pharmaceutical products. The SME will be responsible for overseeing and ... lead training programs, optimize systems, lead harmonization of visual inspection control strategies across the internal and external manufacturing network, and… more
- GRAIL (Durham, NC)
- …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... a quality culture by driving compliance activities around the Change Control , Planned Deviation, and Complaint Handling/Post Market Surveillance Programs, partnering… more
- Amgen (Holly Springs, NC)
- …system owner for building mechanical systems supporting a large bio- pharmaceutical manufacturing site. Your responsibility includes HVAC and Refrigeration (HVAC/R), ... life safety gas detection systems). + Ensure room pressurization strategy, control , testing, and documentation requirements for GMP classified manufacturing space… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …is well-positioned to successfully emerge as a leading integrated research-based pharmaceutical company. POSITION SUMMARY: This position is responsible for overall ... which includes, but is not limited to, the following systems: Document Control , Electronic Quality Management Systems (Investigation, Change Control , CAPA) and… more
- Lilly (Concord, NC)
- …biology, microbiology, engineering). + 5+ years of experience in pharmaceutical manufacturing operations with preference for parenteral manufacturing + Strong ... requirements. Preferred Attributes: + 7+ years in QA roles within the pharmaceutical or medical device industry. + Experience with GMP systems, including Deviation… more
- Pfizer (Sanford, NC)
- …associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories. + Support environmental monitoring and water ... in manufacturing quality or engineering experience in the biotech or pharmaceutical industry + Fundamental understanding of laboratory instrumentation function and… more
- Actalent (Sanford, NC)
- …Job Description The Scientist will play a pivotal role in the Quality Control Method Transfer and Validation team, supporting method validation activities such as ... CE-SDS + PA800 + Bachelor's, Master's, or PhD in pharmaceutical chemistry with relevant experience + 7-8 years of...Method development + Method transfer + cGMP + Quality control + LIMS + Waters HPLC + Maurice +… more
- Chiesi (Cary, NC)
- …care and consumer-facing self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social ... many other enriching diversities. Chiesi USA Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent… more
- Pfizer (Sanford, NC)
- …records, forms and other related GMP documents. + Assist in maintaining control of documentation to include accurate document history and change revision ... communication and problem-solving skills. + Ability to learn and navigate document control and e-systems to facilitate document routing and approval. + Ability to… more
- Fujifilm (Holly Springs, NC)
- …to ensure CGMP compliance * Oversees deviation investigations, change control evaluations, and continuous improvements within the validation framework, ensuring ... CQV processes and reduce validation cycle times * Ensures proper documentation control and approval processes for all validation deliverables * Manages, coaches and… more