GMP QC Analyst - Pharma Lab (Galway)

PSC Biotech Corporation; Galway; On-site; EUR 42,000 - 54,000; Full time

Job summary

PSC Biotech Corporation in Galway, Ireland, is seeking a QC Analyst for a 12-month fixed-term contract onsite.

You will perform analytical testing on finished products and raw materials, ensure GMP compliance, maintain GLP records, and support the QC team to deliver timely results.

Applicants should have a chemistry-based degree and 4–5 years of pharma QC experience, with knowledge of HPLC/IR/UV and EU GMP/US FDA guidelines.

Qualifications

• Bachelor’s degree in chemistry-based discipline.
• Experience in a pharmaceutical Quality Control laboratory operating under cGLP standards.
• Familiarity with regulatory guidelines including EU GMP and US FDA (preferred).
• Strong knowledge of analytical techniques including HPLC, IR, UV, dissolution and physical testing.
• Excellent verbal and written communication skills.
• Organised, methodical and detail-oriented with a proactive approach.

Responsibilities

• Carry out analytical testing on finished products, raw materials and stability using GMP procedures.
• Perform water analysis and environmental monitoring according to procedures and schedules.
• Inspect incoming materials such as foils, labels, bulk finished goods and injectables.
• Operate, calibrate and maintain laboratory equipment.
• Maintain GLP documentation and records.
• Support the QC testing schedule to achieve customer service levels (>95%).
• Escalate discrepancies or non-conformances as required.
• Coordinate the dispatch of samples for external analysis when necessary.
• Manage relationships with external suppliers/vendors for QC consumables.
• Participate in internal laboratory rota tasks and maintain lab housekeeping and safety.

Skills

Quality control

Analytical testing

HPLC

IR

EU GMP

US FDA familiarity

Education

Bachelor's degree in chemistry

Tools

Microsoft Office

HPLC systems

Lab instruments

Job description

PSC Biotech Corporation in Galway, Ireland, is seeking a QC Analyst for a 12-month fixed-term contract onsite.

You will perform analytical testing on finished products and raw materials, ensure GMP compliance, maintain GLP records, and support the QC team to deliver timely results.

Applicants should have a chemistry-based degree and 4–5 years of pharma QC experience, with knowledge of HPLC/IR/UV and EU GMP/US FDA guidelines.