LSC have a great contract opportunity for a QA Specialist – II to join a market leading, top Ten Biopharmaceutical company based in Cork. The Cork campus specialises in Tabletting, Solid Dose, Packaging & Distribution of a range of products.
If you have 4+ years of relevant experience in a GMP environment related field and a BS or 2 + years of relevant experience and a MS and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Performs a wide variety of activities to ensure compliance with applicable regulatory requirements.
o Assists in the completion of Manufacturing related customer complaint investigations.
o Participates in developing and approving Standard Operating Procedures (SOPs).
o Reviews GMP records generated by the Manufacturing and Engineering departments.
o Review and approval of GMP Deviation investigations and CAPAs.
o Performs internal audits and walkthroughs on behalf of the QA department to ensure site compliance to GMP.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o 4+ years of relevant experience in a GMP environment related field and a BS.
o 2 + years of relevant experience and a MS.
o Prior experience in pharmaceutical industry is preferred.
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!
To apply, submit your CV via this advert or contact Ciaran Murphy if you have anymore questions about this QA Specialist – II opportunity!