Hybrid QA Specialist Pharma Quality and Supplier Oversight

Life Science Recruitment; Leinster; Hybrid; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

Life Science Recruitment is seeking a QA Specialist for an award-winning pharmaceutical organization based in Carlow. This is a 11-month contract with hybrid work and daily in-office presence in Carlow.

The role covers supplier management oversight, quality agreements, and documentation validation for new products and materials. A scientific degree and 3–5 years in quality are preferred, with cGMP/GDP knowledge.

Qualifikationen

• Bachelor's degree or higher in a related Science discipline.
• 3-5 years of experience in a quality role, ideally in a pharmaceutical manufacturing environment.
• Knowledge of regulatory/code requirements related to Irish, European, and International Standards.
• Familiarity with cGMP and GDP is preferred.
• Strong report, standards, and policy writing skills.
• Experience with equipment and process validation.
• Familiarity with sterile filling processes and equipment.

Aufgaben

• Supplier management oversight and APR Quality Agreement ownership.
• Review documentation for new product/material introduction (Packs, specs, BOMs, supplier qualification).
• Develop and monitor supplier performance metrics and participate in supplier reviews.
• Maintain the approved supplier management list for Carlow site.
• Support deviation, CAPA, change controls, and supplier complaints.
• Provide quality oversight for technology transfer, method qualification and validation.
• Ensure site compliance with divisional policies and regulatory requirements.
• Participate in cross-functional teams for product introductions.

Kenntnisse

Quality management

Regulatory understanding

Documentation skills

Cross-functional collaboration

Ausbildung

Bachelor's degree in Science

Jobbeschreibung

Life Science Recruitment is seeking a QA Specialist for an award-winning pharmaceutical organization based in Carlow. This is a 11-month contract with hybrid work and daily in-office presence in Carlow.

The role covers supplier management oversight, quality agreements, and documentation validation for new products and materials. A scientific degree and 3–5 years in quality are preferred, with cGMP/GDP knowledge.