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
- Support laboratory setup and equipment qualification.
- Prepare and review laboratory procedures, protocols, and reports.
- Perform QC testing in line with SOPs, cGMP, and regulatory requirements.
- Conduct method verification, validation, and technical transfers.
- Manage laboratory consumables and ensure proper tracking.
- Assist in regulatory audits and maintain audit readiness.
- Collaborate with cross-functional teams, including technicians, operations, and warehouse staff.
- Maintain compliance with Good Documentation Practice (GDP) and Quality Management Systems (QMS).
- Ensure EHS standards are upheld in the laboratory.
- Liaise with CROs and conduct audits as needed.
Requirements
- Degree in Chemistry, Biochemistry, Pharmaceutical Science, or related field.
- Experience in a cGMP-regulated QC or ARD laboratory.
- Strong understanding of method validation, technical transfer, and regulatory compliance.
- Excellent documentation, reporting, and communication skills.
- Ability to manage multiple tasks in a fast-paced environment.
Benefits
- Competitive salary & annual bonus
- Flextime options for work-life balance
- Laya Healthcare for employee, partner & dependents
- 5% employer-matched pension plan
- Educational assistance & career development support
Interested? Apply now and be part of an innovative and high-performing team!
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