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Description
Job Description Your Key Responsibilities: Your Responsibilities Include, But Not Limited To Stewardship: ensure robust product stewardship for all products manufactured at the platform / cluster, and end-to-end technical oversight of product manufacturing processes, at all stages of their commercial lifecycle; provide strong technical leadership to ensure product and related packaging operations are maintained in compliance with current GMP and regulatory requirements; ensure that all manufacturing processes are robust respectively process improvement projects acc. to project plan are implemented; provide governance of platform Manufacturing Robustness Review Board (MRRB). Oversee and ensure the robustness and capability of manufacturing and packaging processes by monitoring of each product’s Critical Process Parameters (CPP) and Critical Quality Attributes (CQAs) thru a continued process verification program and review of Annual Product Reviews (APRs)/Product. Ensure the robustness of manufacturing and packaging processes, so that all site products are validated and remain in constant state of validation throughout the product lifecycle. Ensure single point of contact for products within the site and across sites for multi-site products, as far as process technical issues are concerned. Safeguard, maintain and develop the scientific information of product processes. Support and, were appropriate, lead optimization of pharmaceutical processes by applying sound scientific reasoning (first principles) and following integrated process and technology strategies, triggering post launch development, when needed. Essential Requirements What you’ll bring to the role: Education (minimum/desirable): MSc. In Science, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent experience. Ph.D. desirable. Minimum 15 years’ experience in manufacturing. Additional specialist experience is preferred (e.g. pharmaceutical formulation, process development, manufacturing technology). Cross Cultural Experience. Strategy Development. Leading large and/or diverse multi-functional teams. People Leadership. Collaborating across boundaries. Operations Management and Execution. Skills Change Management. Manufacturing Process Science. Manufacturing Technologies. Npd (New Product Development). Process Simulation. Project Management . Quality Compliance. R&D (Research And Development). Technical Leadership. Why Sandoz? Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more! With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably. Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged! The future is ours to shape! Commitment To Diversity & Inclusion We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Show more Show less
