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 has a long-standing footprint in Ireland with over 3,000 employees across multiple sites and invests heavily in manufacturing biologics-based medicines.
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 compliance and documentation
Quality operations in biotech industry
Review and approval of batch records
Support for commissioning and qualification
Cross-functional team collaboration
Continuous improvement initiatives
Nice-to-have
Strong interpersonal and communication skills
Leadership and problem-solving abilities
Bioprocessing knowledge upstream and downstream
Analytical and critical thinking skills
Key Requirements
Bachelor’s degree in scientific or engineering field or relevant experience
Minimum 5 years post-degree experience in GMP manufacturing or QA
At least 2 years experience in biotech QA operations