3 technical writing jobs found

Validation Associate III Apply   locations San Diego, CA, USA   time type Full time   posted on Posted 4 Days Ago   job requisition id JR117232 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.     Summary: Under minimal supervision, the Validation Associate III performs complex validation and qualification activities for critical equipment, utilities, and processes used in Drug Product Manufacturing, Quality Control Chemistry, and Microbiology. Essential Duties and...

Analytical Technologies Associate I Apply   locations San Diego, CA, USA USA_CA_San Diego_Lusk   time type Full time   posted on Posted 14 Days Ago   job requisition id JR117079 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.     SUMMARY: The Analytical Associate I develops, qualifies, validates, and transfers analytical methods to support drug product and drug substance manufacturing and fill-finish including release and stability testing.  The...

Manufacturing Investigator I     locations San Diego, CA, USA   time type Full time   posted on Posted Today   job requisition id JR117289 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.     SUMMARY: Under direct supervision, this position may investigate, author, coordinate, and revise deviations, corrective and preventative actions, complaints, and other cGMP documents such as Master Production Batch Records. The Manufacturing Investigator I supports simple write-ups and the resolution of...