LSC have a great contract opportunity for a Quality control specialist to join a global Biopharmaceutical company in Carlow. This is a state-of-the-art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia, and infectious disease.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Comply with regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions
- Work collaboratively to drive a safe and compliant culture
- Perform quality function in Quality Risk Assessments as outlined in QRM procedures
- Review and Approve system design documentation in area(s) of responsibility from a Quality perspective
- Pre and Post Approve C & Q test documentation in area(s) of responsibility
- Review and Approve validation summary reports supporting qualification
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
- Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices
- Knowledge of cGMP and GDP
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 Sarina Abdulha at +353 21 4771 329 if you have any more questions about this opportunity!
