LSC have a great contract opportunity for a Quality Assurance Specialist to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 5 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Provide QA oversight of deviations, investigations, CAPAs, and change controls, ensuring timely and compliant execution.
- Review and approve quality records, ensuring appropriate scope, root cause analysis, risk assessment, and corrective actions.
- Represent QA at Deviation Review Boards, Change Control Boards, and other cross-functional forums.
- Support complex investigations and provide quality guidance on compliance and operational issues.
- Monitor quality system trends and support continuous improvement initiatives.
- Contribute to Annual Product Reviews and quality metrics reporting, as required.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology, or a related discipline.
- Minimum 5 years' experience in the pharmaceutical or biotechnology industry.
- Experience providing QA oversight of deviations, investigations, CAPAs, and change controls in a GMP environment.
- Strong understanding of GMP requirements, quality systems, and risk management principles.
- Strong analytical, problem-solving, communication, and stakeholder management skills.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Jenny Murphy on 021 4777329 if you have anymore questions about this role!
