LSC have a great contract opportunity for a QC Associate 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.
If you have 3+ 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:
- Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP
- Facilitate and drive effective communication to ensure success through representation of QC team on tier meetings
- Support all aspects of New Material Introduction process ensuring effective interaction with other departments/global teams/ external contract testing labs on matters related to new material introduction, supplier changes and associated qualification
- Participate and support Internal/External Investigations
- Coordinate the creation/ update to Quality standards for raw materials and components at Carlow. Complete impact assessments for change controls related to Carlow processes
- Coordinate any efficiency/ increased Lab capability projects as detailed by Quality Control Manager
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- 2-4 years of experience in a cGMP laboratory environments
- Knowledge of or previous experience in New Material Introduction process
- Proficiency in Microsoft Office and job related computer applications required
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship. Thank you for your understanding.
Apply via this advert or contact Sarina Abdulha at 0214777329 if you have any questions about this opportunity!
