GMP QA Technical Writer - Documentation Expert

Pace Life Sciences is seeking a Technical Writer for on-site work in Oakdale, MN. You will author, revise, and maintain GMP documentation supporting compliant operations in a regulated lab environment.

Responsibilities include coordinating investigations, CAPAs, change controls, and SOPs, and translating complex data into clear documentation. A Life Sciences/QA/technical communication background is required.

This role is for the GMP QA Technical Writer
- Documentation Expert role at Pacelabs.

We would love to welcome a new GMP QA Technical Writer
- Documentation Expert to our organisation in Oakdale, MN, United States.

For the GMP QA Technical Writer
- Documentation Expert position at Pacelabs, we are reviewing applications now.

Step into the GMP QA Technical Writer
- Documentation Expert role at Pacelabs in Oakdale, MN, United States and grow with us.