Job Title: Quality Assurance Specialist
Location: Cashel, Co. Tipperary
About the Role
A pharmaceutical manufacturing site dedicated to innovation and quality is seeking a Quality Assurance Specialist.
Job Summary
This role involves supporting laboratory setup, conducting essential testing, and ensuring compliance with cGMP standards.
Key Responsibilities
* Support laboratory equipment qualification.
* Develop and review laboratory procedures, protocols, and reports.
* Perform quality control testing in line with SOPs, cGMP, and regulatory requirements.
* Verify, validate, and transfer methods.
* Manage laboratory consumables and maintain proper tracking.
* Assist in audits and maintain audit readiness.
* Collaborate with cross-functional teams.
* Maintain compliance with GDP and QMS.
* Ensure EHS standards are upheld in the laboratory.
* Collaborate with contractors 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 team.
QC Analyst Job Description