Site Program Manager
Pubblicato il 28-08-2026 - Merck Group in Modugno
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. **Your Role**:
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. I'll define and manage the CMC roadmap, identify project milestones, and monitor progression, all while contributing to the site budget with local project cost information. I'll also be instrumental in identifying and managing project risks and issues.
My responsibilities include leading change control for TT and LCM projects, designing new processes, and preparing all necessary technical documentation. I'll 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, I'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 Are**: - Scientific Degree
- At least 2 years in a similar role on a minimo 4 years experience
- Srong 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 spoken **What we offer**: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!