Full-time Posted June 17, 2026
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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.

**Position Title** : QA Specialist II - Document Control

**Location:** Bedford, New Hampshire

**Department:** Quality Assurance, Document Control

**Reporting To:** Supervisor, Document Control

**Responsible For (Staff):** No

The individual will manage, coordinate, and maintain cGMP documentation, procedures, and records to ensure only controlled copies are reviewed, approved, issued, distributed, and archived. The Document Control QA Specialist II will evaluate document needs and participate in the processing of Documents and Records, maintain databases and Quality Management System tools and supports ...

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