LSC have a great contract opportunity for a Complaince Engineer 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.
If you have 2+ years relevant experience in the pharmaceutical industry and/or biotechnology industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Raise CAPA's and conduct investigations. Raise and investigate quality notifications using standard tools and methods, to resolve system issues e.g. FMEA, Fishbone diagrams, 5 why's etc.; implement subsequent corrective action through the change management system.
- Required to comply with Merck Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
- Support and lead Internal Quality audits of Engineering Dept.
- Assist in the management and/or assignment of Engineering training if required
- Work collaboratively to drive a safe and compliant culture in Carlow.
- May be required to perform other duties as assigned.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Experience of working in a cross functional environment.
- Knowledge of and experience in applying Six Sigma and Lean methodologies.
- Positive, flexible action-oriented attitude
- Degree qualification or equivalent Min Level 7 (Science, Engineering, Technical).
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 0214777329 if you have any questions about this opportunity!
