QA Documentation Specialist - Pharmaceutical IndustryLocation: 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 and 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 and 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 ..... full job details .....