Drug Product MSAT and Outsourcing Lead

bJobdescription /bbr /pLocation: Geneva, Switzerland (Minimum 4 days office presence per week)br /Travel Requirements: 20-30% (Includes site visits to European, US, and Asian manufacturing partners)br /Reporting To: Head of Industrial Affairsbr / /ph3Position Summary /h3pWe 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).br /br / /ph3Key Responsibilities /h3pTechnical Stewardship CMO Oversight /pullipAct 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. /p /lilipDrive OTIF delivery of CMC and technical deliverables to CMOs and business partners. /p /lilipMaintain the state-of-validation through process monitoring, APQRs/PQRs, and Continuous Process Verification (CPV). /p /lilipOversee 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. /p /lilipManage budgeted costs for CMOs, including financial forecasting, variance reporting, and cost-benefit analyses for technology transfers and process optimizations. /p /lilipFoster strategic partnerships with external manufacturers through governance frameworks, site visits, and science-based support for lifecycle management. /p /lilipContribute to the continuous improvement of internal processes regarding outsourced manufacturing oversight and cross-functional collaboration. /p /li /ulpTechnical Information Management /pullipDevelop and maintain comprehensive technical dossiers for all assigned products (manufacturing process descriptions, process parameters, control strategies). /p /lilipManage the internal repository of critical manufacturing documentation, including CMC dossier components and batch record summaries. /p /lilipProvide technical input and regulatory strategy recommendations for manufacturing-related changes. /p /lilipSupport the management of Health Authority Questions related to manufacturing and Post-Approval Commitments in collaboration with CMOs, SMEs, and Regulatory Affairs. /p /li /ulpQuality Deviation Management /pullipEvaluate major deviations and change controls from a technical perspective, focusing on product quality, risk mitigation, and regulatory compliance. /p /lilipReview Impact Assessments and CAPAs, providing guidance in collaboration with CDMO partners and internal Quality Assurance. /p /lilipParticipate in customer complaint investigations and field failure management related to outsourced manufacturing, escalating critical issues as necessary.br /br /br / /p /li /ulh3Qualifications Requirements /h3ullipExperience: 5+ years in pharmaceutical Drug Product (DP) manufacturing or CDMO management. /p /lilipTechnical Expertise: Strong MSAT background in process development, technology transfer, and validation. Specific expertise in vaccines/biologics (lyophilization and fill-finish) is highly preferred. /p /lilipRegulatory Knowledge: Deep understanding of cGMP requirements, FDA and EMA regulations, and CMC regulatory submissions (CTD Module 3). /p /lilipLeadership Collaboration: Proven ability to lead cross-functional teams, manage CMO relationships, and utilize tools like FMEA/QRM. /p /lilipProblem-Solving: Excellent technical problem-solving skills with a meticulous, data-driven approach to decision-making. /p /lilipCommunication: Exceptional communication and negotiation skills for engaging with external partners and internal stakeholders. Must have technical authority and credibility. /p /lilipLanguages: Fluent in both English and French. /p /lilipMindset: Entrepreneurial, innovative, pragmatic, and solution-oriented. /p /lilipBonus: Experience in Drug Substance (DS) biological manufacturing is considered a strong asset. /p /li /ul