LSC have a great contract opportunity for a QC Bioassay Analyst 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:
- Ensure timely completion of all assigned data processing and reviewing.
- Ensure timely completion of Laboratory Investigation Reports and deviations through site procedures
- Participate in the timely generation of trend data, investigations, nonconformances, validation protocols, reports in support of method validation/verifications and equipment qualifications.
- Participate in QC Tier 1 daily meetings and ensure effective communication of testing progress, deviations etc.
- Peer review testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved.
- Where applicable, review, approve and trend test results.
- Participate in the laboratory aspects of OOS investigations.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- 2+ years of experience in a cGMP laboratory environment.
- Bachelor's Degree or higher preferred; ideally in a science related discipline.
- Knowledge of regulatory/ code requirements to Irish, European and International Codes, Standards and Practices.
- Understanding of Lean Six Sigma Methodology preferred.
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!
