QC Analyst New

apartmentCPL placeTipperary calendar_month 
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!

#L1-DB4

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