The QA Document Control Specialist II (GMP) supports the cGMP Document Control and Records Management functions for the BMS Bothell site. This role requires strong communication skills, attention to detail, and the ability to work independently in a fast-paced, highly regulated environment.
Requirements
- Bachelor’s degree required; Library Science a plus
- Minimum of 3+ years of document control and records management experience in a cGMP/FDA-regulated biopharmaceutical or cell therapy environment
- Strong understanding of cGMPs, domestic regulatory requirements, and compliance expectations
Benefits
- Competitive hourly rate: $36.02 – $43.95/hr (W-2 only, no C2C)
- Working Hours: Regular business hours. Tuesday - Saturday or Sunday - Thursday (should be flexible to work either)
- 12-month contract with possible extension
- Health insurance, holiday pay, 401(k) program, and other benefits
- Employee referral bonus program
