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.

**Overall Quality Responsibilities**

+ Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department
+ The Qualified Person is responsible for certifying investigational medicinal products in accordance with requirements of Protocol, Investigational Medicinal Product Dossier (IMPD) and Product specification File (PSF)
+ The compliance of all certified batches to EU Directives, Annex 16 and Annex 13 / Detailed Commission Guidelines where applicable for Investigational Medicinal Products (IMPs).
+ Provide the Quality management team direct support and guidance in all quality matte...