Drug Product MSAT Process Specialist

Description du poste

MANPOWER AG – Your career, our focus! Become part of our network and take advantage of countless opportunities! ManpowerGroup is the world's leading company for workforce solutions. With our three brands – Manpower, Experis, and Talent Solutions – we support companies from various industries with their recruitment needs. For 75 years, we have been operating in over 75 countries and accompany our clients throughout Switzerland to successfully carry out their tasks and projects. Show more About the job About the role For our customer in Basel, we are looking for an experienced Drug Product MSAT Process Specialist who will act as a key technical interface between global MSAT and internal as well as external manufacturing sites. This position is focused on supporting the successful industrialization and lifecycle management of drug product processes across the manufacturing network. The role combines process expertise, technical troubleshooting, transfer support, validation activities, and cross-functional coordination. You will contribute to both product-specific and broader network-related initiatives, helping to ensure robust, compliant, and sustainable manufacturing operations. This is a highly visible role requiring strong technical depth, a hands-on mindset, and the ability to collaborate with stakeholders across multiple functions and seniority levels. Key responsibilities Support process industrialization activities across manufacturing sites, including technical readiness, manufacturability assessments, and PPQ-related support Partner with Product Technical Leads and Product Stewards to identify process gaps, evaluate risks, and define appropriate mitigation measures Drive ongoing process optimization and technical product health improvements based on product and portfolio needs Contribute to second source and change source strategies to strengthen supply continuity and process resilience Provide technical support for engineering runs, technical runs, and process-related studies at internal and external sites Act as second-level commercial product support for investigations, CAPAs, troubleshooting activities, and root cause analyses Lead selected non-product-specific investigations and technical problem-solving activities within the manufacturing network Coordinate validated state support activities such as sampling concepts, study material coordination, and additional technical assessments Work closely with pilot plant teams to enable scale-down or real-life experiments supporting transfers, validation work, and process improvement initiatives Ensure the implementation of technical and network-wide initiatives in alignment with site priorities Support lifecycle activities across products, from development through commercial supply and long-term robustness improvements Contribute to complaint-related technical assessments and the deployment of corrective and preventive actions across sites or product groups Drive technical sustainability and digital improvement initiatives related to products, processes, and manufacturing technologies Collaborate closely with global MSAT, site functions, manufacturing leadership, and external partners where required Translate business and technical process needs into digital improvement opportunities together with digital and strategy teams Candidate profile The ideal candidate brings a solid scientific or engineering background combined with practical experience in pharmaceutical process support, validation, or technology transfer. You are comfortable working in a complex manufacturing environment and can communicate technical topics clearly to both operational teams and senior stakeholders. Requirements Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, or a related discipline At least 3 years of relevant industry experience in technical process development, process engineering, process validation, technology transfer, or manufacturing support within pharma or biotech Strong understanding of pharmaceutical quality systems and relevant industry guidelines in process development and manufacturing Good knowledge of regulatory expectations and health authority requirements Hands-on familiarity with platform-specific technologies, manufacturing processes, and production equipment Strong communication skills with the ability to present technical topics in a clear and structured way Fluent English is required; German is considered an advantage Willingness to travel approximately 10% General information Start date: asap Latest possible start: 01.06.2026 Planned duration: until 30.09.2026 Extension: likely Workload: 80–100% Location: Basel Home office: up to 30% Travel: approx. 10% Team size: 12 Working hours: standard Department: Global MSAT DP Process Stewards What makes this role interesting This opportunity offers a broad technical scope across industrialization, validation support, troubleshooting, process robustness, lifecycle management, and digital improvement. It is well suited for professionals who enjoy working at the intersection of science, engineering, manufacturing, and cross-site collaboration in a highly regulated pharmaceutical environment.