Site Project Manager

vor 3 Monaten

CorsiersurVevey, Schweiz Merck Group Vollzeit

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**

Whithin the DS Manufacturing - MSAT department, you are in charge of leading site activities related to the manufacturing of Drug Substance. As such, you represent Vevey site manufacturing in the CMC team and you are the contact point concerning clinical and/or commercial molecule(s) for internal and external relationships.

In your role, you lead projects tasks throughout the lifecycle of a DS manufacturing process (technology transfer, process validation, commercialization, lifecycle management etc.), coordinate replenishment campaigns, lead optimization and/or improvements projects, and support related regulatory activities (dossier submission and/or variation) in line with CMC requirements. You also coordinate production troubleshooting/investigation if required

You ensure the coordination of projects falling under the responsibility of MSAT as agreed with senior management, within agreed scope, time and quality.

You contribute to project strategy elaboration with CMC team, and establish and execute the project plan in collaboration with all involved parties in line with CMC project timelines and budget.

**Who you are**:

- Degree in biotechnology, chemical engineering, or related topic.
- Experience in international pharma or biotech companies, in manufacturing or R&D (3-5 years).
- Experience in leading projects and project teams.
- Sound awareness of current GMP guidelines and knowledge and/or exposure to regulatory requirements and submissions (IMPD/IND/BLA)
- Success record in working in a matrix project management approach
- Excellent planning and organizational skills
- Excellent communication skills; ability to develop constructive relationship with all departments as well as with other sites and companies/partners
- Fluent in English & French - both spoken and written

**What we offer**:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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

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