Quality Technician
Location:Co. Carlow
Shift Pattern: 4-shift rotation
Industry: Pharmaceutical / Sterile Manufacturing
We are partnering with our Client, aleading pharmaceutical company, inseeking an experienced Quality Assurance Specialist to join their dynamic team within a sterile manufacturing environment. This role is crucial in maintaining GMP compliance and supporting production through proactive quality oversight.
Key Responsibilities:
* Provide QA support to manufacturing teams to ensure cGMP and regulatory compliance (EU/US).
* Conduct timely reviews of batch documentation, investigations, and reports.
* Respond swiftly to unplanned events and technical issues on the shop floor.
* Support audit readiness through regular metric tracking and spot checks.
* Participate in complaint investigations and product quality reviews when needed.
* Collaborate cross-functionally to drive continuous improvement using Six Sigma tools.
Key Requirements:
* Experience in a sterile manufacturing or pharmaceutical environment.
* Strong knowledge of cGMP, regulatory standards, and quality systems (e.g., SAP, MES, TrackWise).
* Ability to prioritize, manage multiple tasks, and meet tight deadlines.
* Comfortable working in a shift-based role.
This is an excellent opportunity to join a global leader and play a key role in delivering high-quality, compliant products to market.
Apply now to take the next step in your QA career, email your CV to rachel.ginnell@forcerecruitment.com.
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