This role provides direct Quality support to the Upstream production area as part of a Quality Integrated Product Team in a Biotech facility in Dublin
Job Summary
This role provides direct Quality support to the Upstream production area as part of a Quality Integrated Product Team in a Biotech facility in Dublin.
The Quality Specialist ensures compliance with Good Manufacturing and Documentation Practices and represents quality on the shop floor during shift work.
The company operates multiple sites in Ireland with a strong focus on advancing manufacturing excellence and R&D to impact healthcare globally.
Matching Summary
This role provides direct Quality support to the Upstream production area as part of a Quality Integrated Product Team in a Biotech facility in Dublin.
Skills & Requirements
Must-have
GMP Manufacturing Compliance
Quality Operations in Biotech
Review and Approval of Batch Records
Shop Floor Quality Support
Change Management and CAPA
Regulatory Compliance Support
Nice-to-have
Leadership and Team Collaboration
Continuous Improvement Initiatives
Analytical and Critical Thinking Skills
Bioprocessing Knowledge
Problem Solving and Innovation
Key Requirements
Bachelor’s degree in scientific or engineering field preferred
Minimum 5 years GMP Manufacturing or QA experience
At least 2 years biotech industry QA operations experience
Experience with GMP documentation and pharmaceutical manufacturing