Location
San Diego
Job Type
Full-time
Posted
July 15, 2026
Job Description
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
This position performs a range of routine and semi-routine QA Raw Materials activities to ensure compliance with Quality Assurance and regulatory requirements. Responsibilities include supporting audits, training programs, and documentation review for GMP operations. The role promotes a compliant cGMP environment by following SOPs and provides quality support for investigations related to GMP manufacturing events. It also generates and reviews documentation for batch disposition and batch record assembly. The individual can work independently, within guidelines, and as part of a team. Additional duties include leading projects and training junior sta...
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
This position performs a range of routine and semi-routine QA Raw Materials activities to ensure compliance with Quality Assurance and regulatory requirements. Responsibilities include supporting audits, training programs, and documentation review for GMP operations. The role promotes a compliant cGMP environment by following SOPs and provides quality support for investigations related to GMP manufacturing events. It also generates and reviews documentation for batch disposition and batch record assembly. The individual can work independently, within guidelines, and as part of a team. Additional duties include leading projects and training junior sta...