Drug Product MSAT and Outsourcing Lead

ppbLocation: /b Geneva, Switzerland (Minimum 4 days office presence per week) /p pbTravel Requirements: /b 20-30% (Includes site visits to European, US, and Asian manufacturing partners) /p pbReporting To: /b Head of Industrial Affairs /p h3Position Summary /h3 pWe are seeking a highly skilled Drug Product Outsourcing Lead to serve as the primary point of contact for our Contract Manufacturing Organizations (CMOs). In this critical role, you will lead cross-functional Virtual Plant Teams to drive operational excellence, ensure compliance, and mitigate supply and quality risks. You will manage technology transfers and ensure the On-Time-In-Full (OTIF) delivery of CMC, technical, and regulatory deliverables while adhering to budget and quality standards. Additionally, you will maintain commercial product licenses and ensure compliance for new market registrations (USA and EU). /p h3Key Responsibilities /h3 h3Technical Stewardship CMO Oversight /h3 ul liAct as the Single Point of Contact (SPOC) and lead cross-functional Virtual Plant Teams for CMOs regarding Drug Product MSAT activities, including process improvements, compliance, and tech transfers. /li liDrive OTIF delivery of CMC and technical deliverables to CMOs and business partners. /li liMaintain the state-of-validation through process monitoring, APQRs/PQRs, and Continuous Process Verification (CPV). /li liOversee manufacturing deviations, change controls, and CAPAs from CMOs, conducting risk-based assessments and root cause investigations while ensuring alignment with cGMP, FDA, and EMA regulations. /li liManage budgeted costs for CMOs, including financial forecasting, variance reporting, and cost-benefit analyses for technology transfers and process optimizations. /li liFoster strategic partnerships with external manufacturers through governance frameworks, site visits, and science-based support for lifecycle management. /li liContribute to the continuous improvement of internal processes regarding outsourced manufacturing oversight and cross-functional collaboration. /li /ul h3Technical Information Management /h3 ul liDevelop and maintain comprehensive technical dossiers for all assigned products (manufacturing process descriptions, process parameters, control strategies). /li liManage the internal repository of critical manufacturing documentation, including CMC dossier components and batch record summaries. /li liProvide technical input and regulatory strategy recommendations for manufacturing-related changes. /li liSupport the management of Health Authority Questions related to manufacturing and Post-Approval Commitments in collaboration with CMOs, SMEs, and Regulatory Affairs. /li /ul h3Quality Deviation Management /h3 ul liEvaluate major deviations and change controls from a technical perspective, focusing on product quality, risk mitigation, and regulatory compliance. /li liReview Impact Assessments and CAPAs, providing guidance in collaboration with CDMO partners and internal Quality Assurance. /li liParticipate in customer complaint investigations and field failure management related to outsourced manufacturing, escalating critical issues as necessary. /li /ul h3Qualifications Requirements /h3 ul libExperience: /b 5+ years in pharmaceutical Drug Product (DP) manufacturing or CDMO management. /li libTechnical Expertise: /b Strong MSAT background in process development, technology transfer, and validation. Specific expertise in vaccines/biologics (lyophilization and fill-finish) is highly preferred. /li libRegulatory Knowledge: /b Deep understanding of cGMP requirements, FDA and EMA regulations, and CMC regulatory submissions (CTD Module 3). /li libLeadership Collaboration: /b Proven ability to lead cross-functional teams, manage CMO relationships, and utilize tools like FMEA/QRM. /li libProblem-Solving: /b Excellent technical problem-solving skills with a meticulous, data-driven approach to decision-making. /li libCommunication: /b Exceptional communication and negotiation skills for engaging with external partners and internal stakeholders. Must have technical authority and credibility. /li libLanguages: /b Fluent in both English and French. /li libMindset: /b Entrepreneurial, innovative, pragmatic, and solution-oriented. /li libBonus: /b Experience in Drug Substance (DS) biological manufacturing is considered a strong asset. /li /ul /p #J-18808-Ljbffr