LSC have a great contract opportunity for a QC Compliance Specialist to join a Limerick based Biotech Drug Substance Manufacturing Facility. This is an exciting opportunity to work with next-gen manufacturing technologies, advanced data collection and analysis platforms that will result in safety and quality improvements, increased productivity, and variability reduction. If you have at least 5 years of relevant experience in a cGMP environment and ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Manage and support projects and initiatives aimed at identifying opportunities for improvement in quality and compliance standards Implementing, monitoring, maintaining, and improving the systems and processes used for Quality compliance. Roll out of site quality initiatives. Supporting departmental colleagues and partnering lines with guidance on documentation, compliance issues and systems support. Working proactively to ensure delivery of on-time high quality records, investigations, and associated actions. Monitoring metrics and trends to improve compliance standards that will meet internal and external auditor expectations. Lead and support quality-based investigations and associated action outcomes, including on time completion. ABOUT YOU - ARE YOUR SKILLS A MATCH? BSC in a science related subject (Micro/Chemistry/ Biochemistry or equivalent preferred) with 5+ years of relevant experience. Experience in quality management systems. A background in Quality Control laboratory processes is preferable. For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available at this time. Thank you for your attention. Apply via this advert or directly at Additionally please contact us at if you have any more questions about this opportunity! Skills: Quality Management Systems Quality Compliance Audit readiness