LSC have a great contract opportunity for a QA Compliance 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.
If you have 7 years' + experience in Quality within the pharmaceutical industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
o Assist global GxP business partners with the creation, review, approval and closure of deviations, investigations, CAPAs, change controls and associated quality risk assessments in compliance with internal and external requirements.
o Create and deliver QMS training (process and technical).
o Create and update of QMS procedural documentation and work instructions.
o Extract and compile QMS data into reports for metrics and analysis.
o Develop and maintain strong relationships with global GxP stakeholders to establish communication channels for feedback and enhanced process understanding.
o Lead and participate in internal forums, for example Change Control Review Board, CAPA Review Board and Communities of Practice.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
o Bachelor's degree in a technical or life sciences discipline (ex. Chemistry, Biology, Biotechnology)
o Prior experience in a Global QA role strongly preferred
o Knowledge of global GCP, GLP, GVP, GMP and GDP requirements for quality systems, medical devices and combination products
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 Katie Brown at LSC on 021-4777329 if you have anymore questions about this QA Compliance Specialist opportunity!
