QA Documentation Engineer

QA Documentation Engineer - Germany, Frankfurt - 12 Months Initial Contract. Looking to take your career to the next level? We’re recruiting for a high-impact pharmaceutical project located near Frankfurt. With major capital investment experience driving various facility build projects. This is a unique opportunity for a QA Documentation Engineer to join a global leader in the life sciences market and play a key role in shaping the future of advanced manufacturing.

What You’ll Do

• Implement, and maintain document control processes aligned with GMP, GDocP, and project requirements.
• Support the development and execution of commissioning, qualification, and validation (CQV) documentation.
• Ensure documentation practices comply with GxP, data integrity (ALCOA ), and internal quality standards.
• Train project and operational staff on documentation standards, templates, and systems.

What you’ll need

• Degree in Life Sciences, Engineering, Quality, or related discipline.
• Experience in a GMP-regulated biotech, pharmaceutical, or medical device environment.
• Strong understanding of GDocP, data integrity, and regulatory expectations for documentation.
• Hands-on experience with document control systems (e.g., Veeva Vault, Kneat, Eida Track Wise,).

Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!