Change Management Sr Analyst

Change Management Sr Analyst- Temporary Position   At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where, Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice. When you show proactivity and ambition, we’ll harness it through a variety of opportunities and challenges in the diverse areas of our business – all with a strong and meaningful purpose. Where do you want to go? What do you want to do? How do you want to make a difference? The choice is yours, and we’ll help you get there. Be better together. Be Bayer. Main purpose : Ensure that any proposed changes to the site's GMP environment (processes, equipment, analytical methods, suppliers, etc.) for the business are systematically evaluated, approved, implemented and/or migrated in an agile and efficient way, minimizing risks and ensuring compliance with Bayer's procedures and policies, and all regulations of the supplied markets. Your mission will be to: Manage the change control process for equipment, environment, services, products, processes, packaging and raw materials on the site. Ensure that any change that may affect operational continuity, material availability, production capability, or regulatory compliance is properly identified, assessed, controlled, and documented within the Change Control system, minimizing risks to product quality, supply reliability, and patient/customer impact. Cross‑functional coordination tomaintain supply continuity, anticipate potential risks and establish mitigation plans. Collaborate closely with TPI, Quality, Planning, Controlling, Production and Engineering to ensure changes can be implemented without affecting material flow or manufacturing capability. Monitor implementation of supply‑critical changes and provide visibility of changes that impact key materials, utilities, suppliers, or processes to the Business Continuity. Follow-up on actions and due dates to guarantee on‑time implementation. Track reports and update KPIs related to task and change status. Ensure compliance processes in the sector: self-inspections of processes, SOPs, change controls and CAPAs resulting from audits, deviations, technical support for product registration. Comply with the safety and environmental culture in all site operations, from the design of processes and products, ensuring that processes and products ensure an accident-free environment. Unlock your potential: Degree (graduate) in Chemical or Food Engineering, Pharmacy, Biochemistry or Biotechnology At least 2-3 years of experience in pharmaceutical industry in areas such as Production, Quality, Engineering, etc Background in technical requirements for pharmaceuticals for human use & galenic development is mandatory. Must be able to fluently read, write, and speak English (B2 minimum); ability to attend English calls and make oral presentations fluently. Basic knowledge in the implementation of continuous improvement tools (lean manufacturing) in supporting areas; mindset in digitalization processes. Personal computer (PC) skills required, including advanced skills in Microsoft Excel & SAP. Strong understanding of Data Integrity principles and GDP Ability to lead cross-functional meetings, strong communication, planning, and documentation skills. This is a temporary position (6 to 12 month).