QA Operations Specialist (Temp) – Onsite, Limerick

Regeneron Pharmaceuticals, Inc.; Limerick; Presencial; EUR 42.000 - 65.000; Jornada completa

Descripción de la vacante

Regeneron Pharmaceuticals, Inc. in Raheen, Limerick seeks a Temp QA Specialist to join the QA Operations Batch Review team. You will provide QA oversight for manufacturing, partner across functions to resolve issues, triage non-conformances, and review critical manufacturing documentation.

You will lead investigations, support CAPA, and mentor teams on QA processes, ensuring compliance and high-quality release decisions. On-site role with potential for professional growth.

Formación

• QA oversight of manufacturing operations
• Review and approve manufacturing documentation
• Lead investigations and CAPA activities
• Provide QA mentorship and training
• Support product disposition and release processes
• Ensure documentation aligns with regulatory expectations

Responsabilidades

• Provide QA oversight in production areas
• Coordinate with cross-functional teams to resolve issues
• Triage non-conformances with complete documentation
• Review area clearances, incursions, changeovers, investigations
• Participate in shift meetings and quality improvements
• Guide investigations and corrective actions with QA input
• Support training and development in QA processes
• Review manufacturing records for product disposition/release
• Identify opportunities for continuous improvement

Conocimientos

QA oversight

Cross-functional collaboration

Documentation review

Investigations

Training & mentoring

Quality systems

Attention to detail

Educación

BS/BA in scientific discipline

MS in scientific discipline

Herramientas

Document management systems

CAPA systems

Descripción del empleo

Regeneron Pharmaceuticals, Inc. in Raheen, Limerick seeks a Temp QA Specialist to join the QA Operations Batch Review team. You will provide QA oversight for manufacturing, partner across functions to resolve issues, triage non-conformances, and review critical manufacturing documentation.

You will lead investigations, support CAPA, and mentor teams on QA processes, ensuring compliance and high-quality release decisions. On-site role with potential for professional growth.