LSC have a great contract opportunity for a QA Specialist to join a South Dublin based Biopharmaceutical company that specialises 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 compliance with GMP requirements.
- Review and approve quality records, including root cause analysis, risk assessments and corrective actions.
- Represent QA at Deviation Review Boards, Change Control Boards and cross-functional meetings.
- Support complex investigations, providing quality guidance to Manufacturing, Engineering, Validation and QC teams.
- Monitor quality system trends, support continuous improvement initiatives and contribute to quality metrics reporting.
- Support internal audits, regulatory inspections and inspection readiness activities.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology or a related discipline, with 5+ years' experience in the pharmaceutical or biotechnology industry.
- Strong GMP Quality Assurance experience, particularly in deviations, investigations, CAPAs, change controls and root cause analysis.
- Excellent analytical, problem-solving, communication and stakeholder management skills, with the ability to work independently in a cross-functional environment.
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 Andrea McSweeney on 021 4777329 if you have any more questions about this role!
