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 021 4777329 if you have any more questions about this role!
