QC Analyst – 4‑Shift Rotation – Cork

About the role

We are seeking a Quality Control (QC) Analyst to join a leading global pharmaceutical manufacturing site in Cork. The role is fully onsite and operates on a 4‑shift rotation to support 24/7 manufacturing activities in a highly regulated GMP environment.

Key responsibilities

• Perform primary review of QC raw data and trend analytical results.
• Evaluate analytical and microbiological test results against established specifications.
• Prepare protocols, technical reports, summaries, and regulatory documentation.
• Draft, review, and update QC Standard Operating Procedures (SOPs).
• Conduct laboratory investigations and document findings through to completion.
• Act as a technical Subject Matter Expert (SME) and support the training of colleagues.
• Maintain laboratory compliance and audit readiness at all times.
• Support regulatory inspections and interact with inspectors during audits.
• Collaborate with cross‑functional teams including Manufacturing, Quality Assurance, Facilities, and external partners.
• Contribute to continuous improvement initiatives, standard work practices, and 5S activities.

Required profile

• BSc in a Scientific or Engineering discipline with 5+ years of cGMP laboratory experience, OR MSc in a Scientific discipline with 3+ years of cGMP laboratory experience.
• Strong understanding of GMP regulations and laboratory compliance requirements.
• Experience reviewing analytical data and conducting laboratory investigations.
• Excellent written and verbal communication skills.
• Strong attention to detail with a focus on quality and accuracy.
• Ability to work effectively in a fast‑paced manufacturing environment.
• Proven ability to work collaboratively within a high‑performing team.
• Flexible, adaptable, and committed to continuous improvement.

Required skills

• cGMP laboratory experience
• Analytical testing
• Microbiological testing
• Data review and trend analysis
• Laboratory investigations
• SOP development and maintenance