I have an exciting opportunity for an experienced QC Analyst (Chemistry) to join an expanding company in Tipperary. The successful applicant will 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. Significant pharmaceutical industry experience performing analytical methods such as HPLC, GC, KF, compendial methods, particle size analysis etc is essential for this role.
This is a permanent role fully on site.
Responsibilities will include:
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.
Qualifications & Experience:
Degree in Chemistry, Biochemistry, Pharmaceutical Science, or related field.
2+ years' 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.
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