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Responsibilities:
* Manage the life cycle of all documentation
* Be the point of contact for clients and engineers alike
* Responsible for the timely, accurate and efficient management and implementation of documents including access and revision control
* Drive the Documentation life cycle to ensure schedules are met and quality is maintained
* Work closely with subject matter experts, engineering project teams, support teams, and other stakeholders to create, maintain and approve high-quality documentation
* Effectively manage documentation projects and deliver customer-focused documentation
* Creation and revision of Standard operating procedures (SOPs) as required
* Ensure compliance with all regulatory GMP, Safety and Environmental requirements
* Participate and comply with Quality Management System (QMS) requirements
Ideal Candidate:
* 5+ years experience in Office Administration
* Experience working with GMP Documentation Management Systems and/or a willingness to learn GMP validation documentation development
* Experience in a regulated industry (Pharmaceutical, Manufacturing, Quality, Tech Services) would be advantageous but not essential
* Proficient in Microsoft Office (Word, Excel, PowerPoint)
* Highest level of attention to detail and fast delivery
* 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.
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