GMP QA Specialist - Batch Release & Compliance

DPS Group Global; Waterford; On-site; EUR 52,000 - 72,000; Full time

Job summary

Arcadis are seeking a Quality Assurance Specialist to join a leading biopharmaceutical manufacturing facility in Waterford. The successful candidate will provide day-to-day quality oversight and support to manufacturing operations, ensuring GMP compliance and product disposition in a highly regulated environment.

Reporting to the QA Team Leader, you will collaborate with Production, QC, Engineering and Regulatory teams to support investigations, CAPA, audits, and continuous improvement

Qualifications

• Bachelor's degree in science, engineering, biotech, microbiology or related field.
• GMP-regulated manufacturing experience.
• Experience in QA, QC or manufacturing support.
• Experience reviewing quality documentation and investigations.
• Strong communication and stakeholder management.

Responsibilities

• Provide QA support to manufacturing and operations.
• Ensure products are manufactured per cGMP and regulatory expectations.
• Act as QA representative for assigned processes and systems.
• Support batch release and product disposition.
• Maintain audit readiness and participate in audits.

Skills

QA oversight

GMP

Documentation

Regulatory knowledge

Problem-solving

Education

Bachelor's Degree in Science

Biotechnology

Microbiology

Tools

eQMS

Deviations Tracking

CAPA

Change Controls

Job description

Arcadis are seeking a Quality Assurance Specialist to join a leading biopharmaceutical manufacturing facility in Waterford. The successful candidate will provide day-to-day quality oversight and support to manufacturing operations, ensuring GMP compliance and product disposition in a highly regulated environment.

Reporting to the QA Team Leader, you will collaborate with Production, QC, Engineering and Regulatory teams to support investigations, CAPA, audits, and continuous improvement