Job Responsibilities:
1. Manage the life cycle of all documentation.
2. Be the point of contact for clients and engineers alike.
3. Responsible for the timely, accurate, and efficient management and implementation of documents including access and revision control.
4. Drive the Documentation life cycle to ensure schedules are met and quality is maintained.
5. Work closely with subject matter experts, engineering project teams, support teams, and other stakeholders to create, maintain, and approve high-quality documentation.
6. Effectively manage documentation projects and deliver customer-focused documentation.
7. Creation and revision of Standard Operating Procedures (SOPs) as required.
8. Ensure compliance with all regulatory GMP, Safety, and Environmental requirements.
9. Participate and comply with Quality Management System (QMS) requirements.
Ideal Candidate:
1. 5+ years experience in Office Administration.
2. Experience working with GMP Documentation Management Systems and/or a willingness to learn GMP validation documentation development.
3. Experience in a regulated industry (Pharmaceutical, Manufacturing, Quality, Tech Services) would be advantageous but not essential.
4. Proficient in Microsoft Office (Word, Excel, PowerPoint).
5. Highest level of attention to detail and fast delivery.
6. Experience of ISO would be advantageous.
Salary is based on qualifications and experience and is in the region of €35 – €40,000. If you are interested, please apply or email.
#J-18808-Ljbffr