Job Title: Senior Manager – Late-Stage Process Transfer ValidationLocation: Spain (Hybrid/Flexible Options Available)Company: (Confidential – Mid-Size CDMO Specializing in Drug Product Development Manufacturing)________________________________________About UsWe are a dynamic, mid-sized Contract Development and Manufacturing Organization (CDMO) located in Spain, supporting global pharmaceutical and biotech clients from clinical development through commercial supply. With a strong focus on injectables, aseptic fill-finish, and complex drug products, we blend scientific excellence with operational agility.As we continue to grow our late-stage and commercial manufacturing capabilities, we're seeking a passionate and experienced Senior Manager of Process Transfer Validation to lead key tech transfer and validation programs, ensuring seamless scale-up and GMP readiness.________________________________________Your RoleAs Senior Manager, Late-Stage Process Transfer Validation, you will be the technical lead for process scale-up, technology transfer, and validation activities for late-phase and commercial drug products. You’ll collaborate cross-functionally with internal teams and client stakeholders to ensure robust, compliant, and timely execution of tech transfer and validation strategies.________________________________________Key Responsibilities• Lead late-stage technology transfer of drug product manufacturing processes (e.g., aseptic fill-finish, lyophilization, complex formulations)• Oversee process validation, including PPQ campaign planning and execution• Develop and manage project plans, risk assessments, and validation master plans• Act as primary technical interface with clients during late-phase development and transfer• Work closely with MSAT, Quality, Regulatory, and Operations to ensure GMP-compliant implementation• Author and review protocols, reports, and regulatory documentation (e.g., BLA/MAA sections)• Support continuous improvement and troubleshooting of existing processes post-validation________________________________________Qualifications• Degree in Pharmacy, Chemical Engineering, Biotechnology or related field (MSc or PhD preferred)• 7+ years of experience in pharmaceutical manufacturing or process development, ideally in a CDMO or multi-product GMP environment• Demonstrated expertise in late-stage development, tech transfer, and process validation• Strong knowledge of EU GMP, ICH, EMA/FDA guidelines• Excellent communication and project management skills• Fluent in English; Spanish is a strong plus________________________________________What We Offer• A key leadership role in a growing international CDMO• Autonomy, ownership, and visibility in high-impact programs• Collaborative, agile culture with direct access to senior leadership• Competitive salary, bonus, and relocation support (if applicable)• Beautiful location in Spain with hybrid working options