Quality Technician
Location: Co. Carlow
Shift Pattern: 4-shift rotation
Industry: Pharmaceutical / Sterile Manufacturing

We are partnering with our Client, a leading pharmaceutical company, in seeking 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.