QC Technician/Data Reviewer
NEW QC Technician/Data Reviewer role with a leading pharmaceutical company in Waterford
The successful candidate will support Production and Quality teams with the collection, review and documentation of manufacturing and QC data required for CPV activities.
You will work closely with Production, QC, Quality and MSAT teams to ensure data is accurate, complete and appropriately documented.
Key Responsibilities
- Collect Production and/or QC data required for CPV activities.
- Support the accurate and traceable collation and review of CPV data.
- Provide support to Production and QC teams during the review phase.
- Assist with process investigations, CAPA and root-cause analysis.
- Work with MSAT and Quality teams to resolve data and documentation queries.
- Ensure documentation and data are maintained in accordance with GMP requirements.
- Support the identification and resolution of data discrepancies or missing information.
What We're Looking For
- Previous experience within a GMP pharmaceutical, manufacturing, QC or Quality environment.
- Understanding of pharmaceutical manufacturing operations.
- Knowledge or exposure to CAPA, process investigations and root-cause analysis.
- Strong attention to detail and accuracy when handling data and documentation.
- Good understanding of GMP documentation practices.
- Ability to work collaboratively with Production, QC, Quality and technical teams.
If you have a background in GMP Production, QC, QA or pharmaceutical manufacturing and are interested in this opportunity, please get in touch.
