A highly skilled QC Chemist is required for a full-time on-site role at our multinational biopharmaceutical client in Cork, Ireland.
The successful candidate will support the testing of finished products across various techniques for solid oral dosage, sterile, and biologic product portfolios.
The Role:
* Review analytical data and documentation to ensure compliance with specifications and protocols.
* Support reviews and investigations for out-of-trend/out-of-specification results.
* Participate in validation and commercial/developmental manufacturing activities.
* Troubleshoot standard instrumentation/test methods.
* Coordinate waste management, LEAN/Operational excellence, and 5S efforts as required.
* Participate in QC and cross-functional projects as needed.
* Assist in the training of QC staff.
* Develop and revise methods, specifications, and SOPs as needed.
Requirements:
* Bachelor's Degree (Level 8) in a relevant Science or technical discipline.
* 2+ years of experience in the pharmaceutical industry.
* Experience with chromatographic separations (UPLC/HPLC) and Empower.
* Working knowledge of GMPs, GLPs, and regulatory requirements for testing and validation pertaining to the pharmaceutical industry.