Job Title: QC Analyst
Location: Cashel, Co. Tipperary
About the Company
A global leader in pharmaceutical manufacturing, our Cashel site is dedicated to innovation and quality. We ensure the highest industry standards while delivering life-changing products worldwide.
Job Summary
We are hiring a QC Analyst to support laboratory setup, conduct essential testing, and ensure compliance with cGMP standards. This role offers an opportunity to work in a fast-paced environment and contribute to key quality operations.
Key Responsibilities
1. Support laboratory setup and equipment qualification.
2. Prepare and review laboratory procedures, protocols, and reports.
3. Perform QC testing in line with SOPs, cGMP, and regulatory requirements.
4. Conduct method verification, validation, and technical transfers.
5. Manage laboratory consumables and ensure proper tracking.
6. Assist in regulatory audits and maintain audit readiness.
7. Collaborate with cross-functional teams, including technicians, operations, and warehouse staff.
8. Maintain compliance with Good Documentation Practice (GDP) and Quality Management Systems (QMS).
9. Ensure EHS standards are upheld in the laboratory.
10. Liaise with CROs and conduct audits as needed.
Requirements
11. Degree in Chemistry, Biochemistry, Pharmaceutical Science, or related field.
12. Experience in a cGMP-regulated QC or ARD laboratory.
13. Strong understanding of method validation, technical transfer, and regulatory compliance.
14. Excellent documentation, reporting, and communication skills.
15. Ability to manage multiple tasks in a fast-paced environment.
Benefits
16. Competitive salary & annual bonus
17. Flextime options for work-life balance
18. Laya Healthcare for employee, partner & dependents
19. 5% employer-matched pension plan
20. Educational assistance & career development support
Interested? Apply now and be part of an innovative and high-performing team
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