QC- Chemistry Role Cork

LSC have a great contract opportunity for a QC In Process Analyst to join a leading pharmaceutical company based in Cork. If you have 1+ years of experience in QC in the medical device, pharmaceutical or related industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: * Achieves competency in laboratory methods and procedures. * Trains other QC analysts in laboratory methods and procedures when required. * Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines. * Executes validation, operation, maintenance, calibration and troubleshooting of equipment and its associated software. * Writes, executes, reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use. ABOUT YOU - ARE YOUR SKILLS A MATCH? * A third level qualification of a scientific/technical discipline is required. * Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. * Builds strong productive relationships. Please note: 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 understand that we are unable to provide visa sponsorship. Thank you for your understanding. Apply via this advert or contact Sarina Abdulha on 021 4777 329 if you have any more questions about this opportunity!