Quality Assurance Documentation Controller
On-siteInveran, Connacht, Ireland
Job Summary
Coordinate and manage the site control of GMP documents, including reviewing changes prior to final approval and managing distribution or retrieval of records. Support batch documentation issuance and reconciliation for manufacturing records, while assisting in the preparation, revision, and review of quality system records. Manage the My University curricula for the QA team, coordinate training with Subject Matter Experts, and oversee the archiving of quality records. Collate and report performance metrics within the QA group and support the management of material master data. This role requires a Bachelor's degree in a science-related discipline and strong organizational skills within a fast-paced pharmaceutical environment.
Required Qualifications
- Minimum of a Bachelor's degree (or equivalent) in a Science related discipline
- Must have excellent attention to detail
- Must have excellent communication (oral & written)
- Must have excellent interpersonal skills
- Ability to handle multiple tasks in a fast paced environment
- Strong organisational and time management skills
- Experience of working with various IT systems and software packages
- Strong working knowledge of Microsoft Office (Word, Excel, PowerPoint etc.)
Desired Qualifications
- Experience within a pharmaceutical/medical device company
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