Principal Analytical Specialist

3 weeks ago


Loughrea, Galway, Ireland beBeeAnalytical Full time €45,000 - €55,000
Quality Control Analyst

We are seeking a skilled professional to join our team as a Quality Control Analyst.

About the Role:
  • The ideal candidate will be responsible for carrying out analytical testing on finished products and raw materials, ensuring compliance with regulatory requirements.
  • They will provide technical support as required by management, working closely with cross-functional teams to ensure seamless operations.

The role involves providing timely analysis of raw materials, finished products, and contract manufactured products with minimal OOS issues. You will conduct incoming inspections of foils, labels, bulk finished goods, and injectables, calibrate and maintain laboratory equipment, and support testing schedules to achieve an efficient QC system.

Responsibilities:
  1. Carry out analytical testing on finished products and raw materials to ensure compliance with regulatory requirements.
  2. Provide technical support to management and cross-functional teams as required.
  3. Conduct incoming inspections of foils, labels, bulk finished goods, and injectables.
  4. Calibrate and maintain laboratory equipment.
  5. Support testing schedules to achieve an efficient QC system.
  6. Maintain laboratory documentation to GLP standards.
  7. Coordinate with team leaders and production for timely reporting and feedback.
  8. Report discrepancies, deviations, or non-conformances and follow up on corrective actions.
  9. Send samples for external analysis when needed.
  10. Participate in audits and liaise with external suppliers/vendors.
  11. Ensure adherence to quality procedures and suggest improvements.
  12. Perform assigned internal rota tasks, maintain good housekeeping, and uphold safety standards.
Required Skills and Qualifications:
  • Bachelor's degree in a chemistry-based discipline.
  • 2–5 years of experience as a QC Analyst.
  • Strong MS Office skills.
  • Experience in a pharmaceutical cGLP environment with knowledge of EU, GMP, and US FDA guidelines.
  • Eligible to work in Ireland.
Benefits:
  • Foster an inclusive environment that supports individuals with disabilities.
  • Develop your skills and career with us.
  • Work in a collaborative and dynamic team environment.