LSC has an exciting opportunity for a APIEM-QA to join a pharmaceutical company in Cork. This will be a dynamic environment that is constantly innovating, relies on cutting-edge technology to deliver life-saving medicines. You will be working in a site that supplies active ingredients through complex chemical synthesis and biotechnology manufacturing processes for a range of therapeutics. This is a chance for you to work with a global company that strives for excellence in every aspect of its operation and has a huge reputation for its diverse working culture.If you have 5 years of experienceworking in the pharmaceutical or biotechnology industryand are ready for your next challenge, this could be the perfect opportunity for youABOUT THE PROJECT - KEY RESPONSIBILITIES:Provide quality oversight of Quality control activities at CMs including being the initial point of contact for all quality-related issues with testing.Provide quality oversight of CM method validation or method transfer activitiesAssist in the establishment and revisions of Quality Agreements with affiliates and customers.Ensure compliance to Quality Agreements and Manufacturing Responsibilities Documents (MRDs).Coordinate and perform quality responsibilities of API shipments for stability testing. Provide quality oversight of API EM stability program.Participate in Joint Process (JPT) and Post Launch Optimization (PLOT) Teams.ABOUT YOU - ARE YOUR SKILLS A MATCH?BS in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences.5+ years of GMP Quality Control Laboratory knowledge and/or experience in API or finished product manufacturing, QA or Engineering.Testing experience with Small MoleculeThorough technical understanding of quality systems and regulatory requirements relating to quality control laboratoriesNote: 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 applyApply via this advert or contact Cian Marnane at LSC on if you have any more questions about this role