Global CMO Clinical Packaging Site Manager
Flexsis AG, Filiale Basel LSDescription of the company
Flexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting.
For our client Roche Diagnostics in Zug, we are looking for a reliable and motivated (m/f/d).
Global CMO Clinical Packaging Site Manager
Start Date: 15.09.2026
Latest Possible Start Date: 01.10.2026
Planned Duration of Employment: 11 months
Extension (for temporary contracts): with approved budget, project extension (possible but not guaranteed)
Role & Responsibilities
- CMO Site Management: Organize and oversee clinical drug labeling, packaging, and device assembly production outsourced to a global network of CMOs.
- Project & Delivery Oversight: Proactively manage CMO project onboarding, communications, timelines, and delivery performance for outsourced clinical packaging orders to meet supply chain needs while adhering to cost and quality standards.
- Procurement & Contracting: Partner with Procurement and key stakeholders to drive Request for Proposals (RFPs) and Statements of Work (SOWs), negotiate supply agreements, and select vendors.
- Strategy & Budgeting: Support leadership in defining supply strategies for non-standard supply chains. Own the budgeting process and submission for CMO project variable costs.
- Process Ownership & Governance: Establish team scope and division of responsibilities with upstream functions (e.g., device CMO team). Define, track, and report CMO team KPIs.
- S&OP Representation: Actively drive network supply outcomes and represent the CMO function in the CD&OP process.
- Managing operational orders, and master data in SAP
Candidate Profile
- Degree: BA/BS degree, preferably in a technical, business, or supply chain discipline. Master's degree is a plus
- Work Experience: 8+ years of experience in the pharmaceutical industry, supply chain management, or manufacturing
- Domain Knowledge: Strong preference for experience in clinical drug manufacturing, clinical supply chain, or contract manufacturing management
- GMP Experience: Required
- IT / Tool Skills: Proficient knowledge and hands-on experience with SAP or equivalent ERP systems
- Language Skills: Excellent written and spoken English (required); basic German skills are beneficial
- Shift Flexibility: Flexibility to adapt to global working hours (e.g., starting as early as 7:00 AM for SSF teams or working until 6:00 PM for Switzerland-based teams)
- Solid understanding of pharma supply chains, contract manufacturing, and clinical operations.
- Proven project planning, project management, and resource management skills.
Have we sparked your interest and would you like to take your chance? Then we should definitely get to know each other! Simply click on "Apply now" and we look forward to receiving your complete application documents.
