QC Analyst

About the Role

As a QC Analyst at our Waterford manufacturing facility, you will join a dedicated Quality Control team committed to producing safe and high-quality pharmaceutical products that positively impact patients worldwide. Operating within a current Good Manufacturing Practice (cGMP) environment, our team prioritizes accuracy, integrity, and teamwork while fostering continuous improvement and professional growth.

Main Responsibilities

• Execute analytical tests efficiently according to planned schedules and timelines.
• Conduct all activities adhering strictly to cGMP and Health, Safety & Environment guidelines, including complying with documented procedures and maintaining proper records.
• Precisely document raw data, calculations, and all related test information to uphold data integrity and cGMP standards.
• Ensure you possess formal qualifications and proper training before performing specific analytical tests.
• Review quality control data generated by colleagues promptly, aligned with the testing schedule.
• Report any quality or safety incidents such as deviations or out-of-specification outcomes immediately to your manager to facilitate appropriate investigations.
• Participate actively in investigative efforts to identify root causes and conduct impact assessments thoroughly.
• Complete any assigned Corrective and Preventive Actions (CAPAs) aimed at remediation and continual process enhancement.
• Maintain laboratory instruments and facilities in a clean, safe, and operational state consistently.

Candidate Profile

• Proven experience in analytical testing within pharmaceutical, biotech, or regulated manufacturing sectors.
• Detail-oriented mindset with excellent collaboration and straightforward communication skills.
• Proactive problem solver capable of managing and prioritizing multiple tasks effectively.
• Sound understanding of cGMP principles and data integrity requirements alongside familiarity with laboratory instruments and analytical methodologies.
• Experience working with quality documentation systems.
• Academic qualification in Science, Chemistry, Pharmacy, or a related discipline, or equivalent hands-on experience.
• Fluent in English.

Equal Opportunity Employer

We are committed to diversity and inclusion, providing equal opportunity employment regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.