Job Description
Description:
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
The Technical Services Specialist has primary responsibility in supporting the cGMP manufacture of biological bulk drug substance (BDS) at company’s facility in Blanchardstown, Dublin. The Technical Specialist will provide processing expertise to support routine commercial manufacturing, technology transfer, and process validation for Downstream manufacturing of new/existing drug substance (DS) manufacturing processes to the Dublin facility. The person will be required to work in close collaboration with Operations, Engineering, Supply Chain, Quality, Quality Control, Regulatory and other involved departments to provide successful process support. The person should have experience in Downstream Purification unit operations, Process Validation (PPQ), Process Monitoring, Risk Assessment (using QRM tools), and building strategies / SME capability.