Sterile GMP QA Specialist | Quality Assurance in Pharma

Life Science Recruitment; Munster; On-site; EUR 40,000 - 60,000; Full time

Job summary

Life Science Recruitment is seeking a QA Specialist for a Sterile Manufacturing site in Waterford, Ireland. You will ensure products are manufactured, stored and packaged in compliance with cGMP and participate in audits and continuous improvement.

The role requires a science-based degree and at least two years of QA or GMP experience; sterile/aseptic manufacturing experience is highly desirable. You will review batch docs, CAPAs and deviations, and provide quality guidance across the site.

Qualifications

• Degree in science, quality, engineering or related discipline.
• Minimum two years in QA or GMP quality role.
• Experience in pharmaceutical/regulated manufacturing environment.
• Strong knowledge of cGMP requirements.
• Sterile/aseptic manufacturing experience desirable.
• Experience reviewing deviations, investigations, CAPAs and batch documentation.

Responsibilities

• Act as quality point of contact for assigned manufacturing systems and processes.
• Provide quality guidance to manufacturing and supporting departments.
• Review batch documentation, investigations and GMP records.
• Identify quality concerns and support their resolution.
• Support deviation investigations and CAPA closures.
• Collaborate to close audit findings and quality actions.
• Assist in procedures, batch records and controlled docs.
• Deliver GMP training packages.
• Perform internal audits and participate in supplier/regulatory audits.
• Monitor Right First Time performance and quality trends.
• Address recurring documentation and compliance issues.

Skills

Quality Assurance

GMP knowledge

Documentation review

CAPA investigations

Internal audits

Education

Third-level qualification in science/quality/engineering or related

Job description

Life Science Recruitment is seeking a QA Specialist for a Sterile Manufacturing site in Waterford, Ireland. You will ensure products are manufactured, stored and packaged in compliance with cGMP and participate in audits and continuous improvement.

The role requires a science-based degree and at least two years of QA or GMP experience; sterile/aseptic manufacturing experience is highly desirable. You will review batch docs, CAPAs and deviations, and provide quality guidance across the site.