QA Specialist

LSC have a great contract opportunity for a Quality Assurance Specialist to join a leading biotech company based in Dublin. If you have 6 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 : Support various site functional and cross functional tier structures. Completes review and approval for CAPAs, change requests, and investigative protocols and final reports. Responsible for the quality aspects of material and supplier management, such as compilation of material qualification pack, supplier audit review, supplier management system upkeep. Involved in the development and review of documentation and quality records in collaboration with other stakeholders such as QC, MS&T, Engineering and Warehouse throughout the product lifecycle e.g. method validation, facility upgrades, qualification protocols, calibration records. Review and approve GMP documentation / data for accuracy and completeness. Working cross functionally to ensure projects milestones are met in a timely manner. ABOUT YOU - ARE YOUR SKILLS A MATCH? Bachelor's degree (or higher) in Chemistry, Biology, Microbiology, Engineering or Supply Chain in a relevant discipline. 5 years' experience in Quality Control, Quality Assurance or Pharmaceutical, Vaccine or Biological Operations, or Technical Operations. Strong knowledge of qualification and implementation of Single Use technologies and raw materials for use in a GMP 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 Cian Marnane at LSC on if you have any more questions about this role! Skills : Deviation CAPA Documentation