Senior External Manufacturing QC Analyst — Pharma

Russell Tobin; Dublin; On-site; EUR 60,000 - 90,000; Full time

Job summary

Russell Tobin is seeking an Analytical Senior Specialist (Pharma) for External Manufacturing Quality in Dublin. The role supports testing of products at external CMOs/CTLs and acts as QC expert across global teams to ensure compliant, timely results.

You will review investigations, lead major analytical deviations, coordinate method transfers, and support audits. A 3–5 year GMP QC background and GMP/FDA/EU knowledge are essential.

Qualifications

• Requires a BA/BSc in life sciences and 3–5 years of GMP QC experience.
• Strong knowledge of worldwide GMP requirements (FDA/EU) and laboratory QMS.
• Hands-on QC testing experience with RSMs, intermediates, API and drug product.

Responsibilities

• Provide analytical expertise and troubleshooting support for external manufacturing.
• Plan and manage testing of pharma products at CMOs/CTLs.
• Review and approve laboratory investigations, deviations and OOS events; support QA functions.

Skills

GMP QC experience

Project management

Troubleshooting

Critical review of investigations

Independent work in matrixed teams

FDA/EU GMP knowledge

Quality management systems

Education

BA/BSc in life sciences

Tools

Electronic document management systems

Deviation management systems

Analytical technical transfers

Third-party relationship management

Job description

Russell Tobin is seeking an Analytical Senior Specialist (Pharma) for External Manufacturing Quality in Dublin. The role supports testing of products at external CMOs/CTLs and acts as QC expert across global teams to ensure compliant, timely results.

You will review investigations, lead major analytical deviations, coordinate method transfers, and support audits. A 3–5 year GMP QC background and GMP/FDA/EU knowledge are essential.