Job Description
Upstream Manufacturing Process Specialist (hybrid) RK0083 Contract 12 months Cork Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. This position is responsible for representing operations on capital project teams and supporting first line troubleshooting of the day-to-day activities within Operations Duties: Represent Operations on cross functional project implementation teams. Monitoring and troubleshooting of the manufacturing process and equipment issues and process optimization Monitoring and reporting of process performance using statistical process control Troubleshooting of DCS (e.g Delta V) and PLC control systems Investigating and resolving issues raised within the Manufacturing Department Participate in/ Lead Cross Functional teams when required. Support of Commissioning and Qualification activities Preparation and updating of Batch Records, Procedures and Work Instructions Provide process and equipment related training as required within the Manufacturing Department Completion of assigned tasks to support manufacture of quality biomedicines in accordance with cGMP and EHS requirements. Experience and Education: Bachelors Degree in a scientific/technical discipline required A minimum of 5 years experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry. Manufacturing experience within a GMP regulated environment. Experience of the cell culture or purification processes and Project / New equipment installation experience Industry experience in upstream fed batch bioreactors. If interested in this posting please feel free to contact Rachel Kent on or for further information. Skills: Upstream Manufacturing Process GMP Delta V