Were currently recruiting for an exciting opportunity with a Pharmaceutical organisation based in Tipperary. This is an excellent position for anyone who is looking to join a leading multinational who are addressing some of the worlds most challenging healthcare needs. Duties: Ownership and management of changes as associated with large strategic large projects. Changes may be related to processes e.g. equipment, automation and supply chain or other technical functions as required. Responsible for initiation, ownership, and management of changes through the change control systems. Preparation and progression of GMP and Non GMP changes in IPI, Vault QMS and Enablon systems. Collaboration with change initiators, subject matter experts, reviewers, approvers, and external manufacturing groups through the life cycle of relevant changes. Obtain approval for change from relevant review board. Impact assessment for relevant changes. Liaise with stakeholders for impact assessment and task identification. Aligning of system release strategy with stake holders/ operations. Identification and implementation of process optimization opportunities where they arise. (e.g. Hierarchy or dependency optimization, material control strategies). Maintaining accurate task scheduling per project requirements. Minimizing the number of overdue tasks through schedule management. Engagement with the tier process to escalate changes or tasks that are off track. Conduct safety and quality walkdowns, as required. Education and Experience: Ideally candidates should have a strong emphasis on change control documentation, a GMP/GDP background and a degree in a science and or engineering based discipline. Minimum of 3-8 years experience with experience of working in a project environment in a pharmaceutical industry. If interested in this posting please feel free to contact Avishek Singh at Avishek.sing or for further information.