Senior QA Packaging Lead - GMP Quality Oversight (Shift)

BioMarin Pharmaceutical Inc.

Ireland

On-site

EUR 42,000 - 58,000

Full time

14 days+

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Job summary

BioMarin Pharmaceutical Inc. is seeking a Senior QA Packaging Associate in Ireland to deliver quality oversight for packaging and finished goods on a shift basis.

The role focuses on ensuring GMP compliance, reviewing batch records, and supporting continuous improvement in packaging operations. The successful candidate will act as the primary Quality contact on shift, coach team members, and participate in cross-functional quality activities to strengthen accountability and right-first-time

Qualifications

  • Degree in scientific, quality, engineering or related discipline.
  • GMP-regulated pharmaceutical/biotech/medical device experience.
  • Experience in Quality Assurance, Packaging Operations, Finished Goods or related GMP support function.
  • Solid understanding of GMP, batch documentation, deviations, investigations, CAPA and Quality systems.
  • Experience leading investigations, RCARs, cross-functional Quality activities desirable.

Responsibilities

  • Provide Quality oversight for Packaging and Finished Goods per GMP and BioMarin procedures.
  • Review and ensure accuracy of Lot Release Packs and packaging batch records."
  • Support Secondary Packaging Operations with Quality presence on the floor.
  • Serve as main Quality contact on shift for escalations and real-time decisions.
  • Coach QA Associates and shift colleagues to improve right-first-time behaviors.
  • Participate in RCARs, deviations, investigations, customer complaints and CAPA.
  • Write/approve GMP documents and maintain quality systems.

Skills

Quality mindset
Stakeholder management
Clear communication
Technical writing
Problem solving

Education

Science/Engineering degree

Job description

BioMarin Pharmaceutical Inc. is seeking a Senior QA Packaging Associate in Ireland to deliver quality oversight for packaging and finished goods on a shift basis.

The role focuses on ensuring GMP compliance, reviewing batch records, and supporting continuous improvement in packaging operations. The successful candidate will act as the primary Quality contact on shift, coach team members, and participate in cross-functional quality activities to strengthen accountability and right-first-time

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