Qa Operations Specialist

med-in.at

Dublin, , Ireland
Quality assurance operations
Gmp compliance and documentation
Batch record review and approval
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 quality and compliance of products manufactured by the functional area, adherence to Good Manufacturing and Documentation Practices, and represents quality on the shop floor.
  • The position involves participation in continuous improvement initiatives to enhance operational efficiency and resolve issues.

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

  • Quality Assurance Operations
  • GMP Compliance and Documentation
  • Batch Record Review and Approval
  • Quality Support for Upstream Production
  • Regulatory Compliance Support
  • Cross-functional Team Collaboration

Nice-to-have

  • Leadership and Mentorship Skills
  • Problem Solving and Critical Thinking
  • Continuous Improvement Initiatives
  • Bioprocessing Knowledge
  • Strong Oral and Written Communication

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 Quality systems and pharmaceutical manufacturing
  • Strong interpersonal and communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter