Job Description
Purpose This role will be instrumental in supporting site Capital & Expense projects. You will work closely with the project team to develop and implement project change control strategies, ensuring seamless and efficient project delivery. Reporting to the Site Projects Lead, you will have the opportunity to collaborate with various stakeholders and drive impactful change across multiple projects. Responsibilities Lead in the development of project change control documentation and facilitate its implementation. Engage with project change control committees to address and resolve any queries. Manage and oversee the change control process, ensuring timely closure of actions. Utilize advanced systems and tools to efficiently process and update project documentation. Ensure compliance and quality by overseeing the handover process from vendors/contractors. Contribute to the maintenance of engineering information systems for effective data tracking and management. Actively participate in various project-related metrics reporting and Tier board updates. Requirements 3rd level qualification in Engineering, Quality, or a related discipline. Proven experience in documentation control within the Pharm/Bio Pharm industry. Extensive understanding of project life cycles and demonstrated experience in project activities. Familiarity with engineering project management tools and systems. Strong knowledge and appreciation of working in regulated GMP environments. Exceptional interpersonal and customer relationship management skills. Excellent communication, presentation, and organizational abilities. Proficiency in utilizing digital platforms and software for effective information structuring and storage. Skills: Change Control Pharmaceutical Project Life Cycles