GMP QC Analyst – Onsite Lab Specialist

PSC Biotech® Corporation; Galway; On-site; EUR 32,000 - 46,000; Full time

Job summary

PSC Biotech in Galway invites a motivated QC Analyst to join our fast-paced Quality Control Department. You will carry out analytical testing on finished products, raw materials and stability using GMP-compliant procedures to meet regulatory standards.

The role is a 12-month fixed-term contract onsite, requiring a Bachelor’s degree in a chemistry-based discipline and 1–2 years’ experience in a GLP/cGLP environment, with exposure to HPLC, IR, UV and dissolution testing.

Qualifications

• 1–2 years of experience in analytical techniques including HPLC, IR, UV, dissolution, and physical testing.
• Experience in a pharmaceutical Quality Control laboratory operating under cGLP.
• Familiarity with EU GMP and US FDA standards (preferred).

Responsibilities

• Perform physical and chemical testing of raw materials, finished products (e.g., tablets, boluses, veterinary drenches), contract-manufactured goods, stability samples, validation lots, and cleaning validation samples.
• Conduct water analysis and environmental monitoring according to relevant procedures and schedules.
• Inspect incoming materials such as foils, labels, bulk finished goods, and injectables.
• Operate, calibrate, and maintain laboratory equipment per calibration/maintenance protocols.
• Adhere to SOPs, pharmacopoeias, specifications, regulatory guidelines, and GLP.
• Maintain laboratory logbooks and documentation in GLP compliance.
• Support QC testing schedule to achieve customer service level >95%.
• Escalate discrepancies and non-conformances, and coordinate sample dispatch for external analysis.
• Manage relationships with external suppliers/vendors for QC consumables.

Skills

Analytical techniques

Team collaboration

Communication skills

Organised

Problem solving

Education

Bachelor's degree (Level 8) in chemistry-based discipline

Tools

Microsoft Office

Job description

PSC Biotech in Galway invites a motivated QC Analyst to join our fast-paced Quality Control Department. You will carry out analytical testing on finished products, raw materials and stability using GMP-compliant procedures to meet regulatory standards.

The role is a 12-month fixed-term contract onsite, requiring a Bachelor’s degree in a chemistry-based discipline and 1–2 years’ experience in a GLP/cGLP environment, with exposure to HPLC, IR, UV and dissolution testing.