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 is a leading healthcare organization in Ireland with over 3,000 employees across multiple sites and significant investment in biologics drug substance manufacturing.
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
Production Documentation Review
Shop Floor Quality Support
Commissioning and Qualification Documents
Continuous Improvement Initiatives
Nice-to-have
Strong Interpersonal Skills
Leadership and Communication Abilities
Analytical and Critical Thinking
Collaboration in Cross-Functional Teams
Problem Solving Skills
Key Requirements
Bachelor’s degree in scientific or engineering field preferred
Minimum 5 years GMP Manufacturing or Quality Assurance experience
At least 2 years biotech industry QA operations experience
Experience with GMP documentation authoring and approval