At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. Youll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxters products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. An exciting opportunity has arisen for a Production Specialist within Supply Chain to join our rapidly growing Compounding Unit at our Baxter Thetford site. You have will have a deep knowledge of and experience with manufacturing processes. You understand the importance of building relationships, establishing order, and maintaining clear communication channels. As a Production Specialist, you are willing to listen and inspire others by your actions, recommend effective ways to improve Supply Chain quality and/or production process improvements. You also appreciate the stability of a large multinational company with a long history of growth and success. Your team is an extension of your family, and you know how to support them as individuals while helping them achieve results as a team. If you are looking to join an organisation that truly makes a difference, then we would love to hear from you. Benefits • 25 days annual leave bank holidays • Employee discount scheme • Blue light card • Progression opportunities • Subsided canteen • Westfield healthcare • Up to 8% pension contribution • Employee assistance programme What youll be doing • Responsible to ensure timely completion of relevant deviation and complaint investigations to identify true root cause. • Works with the functional area to improve or develop standard operating procedures, documenting workflow and process steps. • Participate in Change Control Review Board meetings - where change control progress and current activities are presented, and new proposed changes discussed. • Build relationships with site leadership, the Quality Assurance/Quality Management Systems team and collaboratively identify root causes and opportunities to improve. • Participate in CA/PA Review Board meetings - where investigation progress and current activities are presented and approved. • Implement deviation investigation tools to local production problems, using data analysis to support process improvement plans. What youll bring • Experience in deviation management, corrective and preventative action identification and organisational change processes. • Excellent verbal and formal communication skills, together with critical reasoning skills. • Proactive logical approach to problem solving utilising lean manufacturing techniques.