QC Documentation Controller sought for pharmaceutical client in Waterford, Ireland, to support QC Digital Paperless project and ensure compliance with c GMP requirements.
Key Responsibilities:
- Define, manage, and maintain a documentation control system for QC projects & BAU c GMP documents.
- Manage, index, and control QC on-site and off-site documents.
- Create and maintain QC procedures.
- Train QC site personnel on Documentation Management Processes and QC Luna project implementation.
- Define, manage, and maintain QC project key metrics.
- Support Product Performance Reviews (PPR).
- Support and report right first-time documentation findings.
- Participate in internal audits and external audits.
- Ensure issuance and storage of QC and Projects documents.
Requirements:
- Minimum Level 7 Scientific qualification or accreditation.
- Minimum of 3 years experience in similar role.
- Very good knowledge of c GMP in a regulated environment.
- Excellent accuracy and attention to detail.
- Strong Planning/Organising skill.
About Career Wise Recruitment:
- Established in 1999, Career Wise Recruitment specialises in recruitment of management and technical professionals.
- Operating out of multiple locations in Ireland.