LSC have a great contract opportunity for a QA 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:
- Author Annual Product Review, Trend Reports.
- 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 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.
- Work collaboratively to drive a safe and compliant culture in Carlow.
- May be required to perform other duties as assigned.
- Assist in the management and/or assignment of QC training if required
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- 3-5 years' experience in a quality role (QC/ QA), ideally in a pharmaceutical manufacturing environment.
- Proficiency in Microsoft Office and job-related computer applications required with proven analytical and systematic problem solving skills
- Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices
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.
