As Senior Program Manager, you'll be the linchpin for Technology Transfer (TT) and Life-Cycle Management (LCM) of drug products, ensuring alignment with site and global strategies. You'll be the central point of contact within the CMC Team, guaranteeing seamless communication and information flow. You'll lead and coordinate the CMC roadmap, identify project milestones, and monitor progression, all while contributing to the site budget with local project cost information. You will also be instrumental in identifying and managing project risks and issues. Your responsibilities include leading change control for TT and LCM projects, designing new processes, and preparing all necessary technical documentation. You will support the planning and execution of engineering, PPQ, and commercial launch batches, contribute to CMC dossier preparation, and ensure timely responses to Health Authorities. Finally, you'll help define process control strategies and drive continuous process improvement, always maintaining compliance with Health Authorities' guidelines and upholding Health and Safety rules.Who You AreScientific DegreeAt least 2 years in a similar role on a minimum of 4 years of experienceStrong understanding of drug product life cycles.An exceptional communicator, adept at fostering collaboration across teams.Highly organized and detail-oriented, capable of managing complex projects.Proactive in identifying and mitigating potential project risks.Experienced in preparing comprehensive technical documentation for pharmaceutical processes.Committed to maintaining the highest standards of quality and compliance.Fluent in English, both written and spokenJ-18808-Ljbffr
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