QC Analyst New

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.

• 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.

• 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.

• 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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