QA Documentation Specialist - Pharmaceutical Industry

Location: Maidstone
Full-time Monday - Friday 9am-5pm
Salary £24-30,000
Join a Kent based, localised but global company and play a key role in quality assurance and compliance! An exciting time to join a growing company who are currently expanding!

Why Apply for a role in quality and compliance?

- Innovative & Impactful - Work with cutting-edge solutions.
- Global Standards - Ensure compliance with GMP, MHRA, FDA, and ISO regulations.
- Career Growth - Develop your skills in a supportive, cross-functional team.

Your Role as a Document Manager within Quality and Compliance:

- Prepare, edit, and manage GMP-compliant documentation.
- Support users on the online documentation system.
- Maintain controlled records and assist with compliance & training.

Skills required for this Quality and Compliance Administrative role:

- Strong Microsoft Office skills (Word, Excel, Visio, Access).
- Detail-oriented with QA/Regulatory experience (Pharma/Medical preferred).
- Collaborative mindset, working across multiple departments.
Ready to advance your career? Apply now - confidential applications welcome!

Contact Sarah Gilbertson - (phone number removed) Option 2