This role provides direct Quality support to the Upstream production area as part of a Quality Integrated Product Team, ensuring compliance with Good Manufacturing and Documentation Practices
Job Summary
This role provides direct Quality support to the Upstream production area as part of a Quality Integrated Product Team, ensuring compliance with Good Manufacturing and Documentation Practices.
The position involves active participation in cross-functional projects and continuous improvement initiatives to enhance operational efficiency and resolve issues.
The company operates a dynamic team across multiple Irish sites with a strong footprint in healthcare manufacturing, investing over $6 billion in Irish operations.
Matching Summary
This role provides direct Quality support to the Upstream production area as part of a Quality Integrated Product Team, ensuring compliance with Good Manufacturing and Documentation Practices.
Skills & Requirements
Must-have
GMP Manufacturing Compliance
Quality Assurance Operations
Batch Record Review and Approval
Shop Floor Quality Support
Performance Qualification Activities
Cross-functional Team Collaboration
Nice-to-have
Leadership and Communication Skills
Problem Solving and Critical Thinking
Continuous Improvement Initiatives
Bioprocessing Knowledge
Data Integrity Support
Change Management Experience
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