LSC have a great contract opportunity for Quality Assurance Specialist to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra-rare disorders through the innovation, development, and commercialization of life-transforming therapeutic products
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Provides guidance to global GMP/GDP business partners to support compliant and timely execution of quality management systems (QMS) records such as deviations, investigations, CAPAs, change controls and laboratory investigations.
- Integrates knowledge and experience as skilled specialist with knowledge of corporate and industry standards with respect to area.
- Creates and delivers QMS training and coaching (process and technical).
- Creates, owns, and manages deviations, change controls, and CAPA in Track Wise.
- Creates, updates, reviews, approves and implements QMS procedural documentation and work instructions with accuracy and clarity.
- Completes assigned projects, supporting delivery on time and in full. Provides regular updates on progress.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- 8 years' + experience in Pharmaceutical, Device or Commercial Quality Assurance within the biopharmaceutical or pharmaceutical industry.
- Prior experience creating and delivering training required.
- Direct experience with development and approval of deviations, CAPAs, Change Controls and laboratory investigations.
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 Grainne Hodnett at LSC on 021-4777329 if you have any more questions about this role!
