Project Change Control Engineer

Job Description About PSC Biotech   Who are we? PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.   ‘Take your Career to a new Level’ PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.   Employee Value Proposition Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met. Overview: We are seeking a dynamic and driven individual to join our Site Projects Group as a Project Change Control Engineer .This role will be instrumental in supporting site Capital & Expense projects and will provide an excellent opportunity to work in a diverse and inclusive team environment. As a pivotal member of our team, 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. Requirements Key Responsibilities and Opportunities: 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   Qualifications and Skills: We encourage applications from candidates with a 3rd level qualification in Engineering, Quality, or a related discipline. Additionally, we seek individuals who possess the following skills and knowledge: 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 Requirements We encourage applications from candidates with a 3rd level qualification in Engineering, Quality, or a related discipline. Additionally, we seek individuals who possess the following skills and knowledge: 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