Site Process Lead

Vor 7 Tagen

Darmstadt, Deutschland 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**:
As a Site Process Lead (all genders) at the pharmaceutical manufacturing site in Darmstadt, you will identify and resolve complex manufacturing challenges as an expert.

In your role as project leader, you will drive initiatives to enhance process robustness and support the manufacturing sites. Your responsibilities will include leading supplier qualifications, implementing process improvements, mitigating risks, developing regulatory strategies, initiate necessary change management processes and enhancing product knowledge. You will manage projects with international experts within cross-functional teams and interface with various business functions. By leveraging innovative, science-driven solutions, you will optimize processes in a GMP environment to ensure a reliable supply for patients.

Additionally, you will develop process control strategies (PCS) and conduct continued process verifications (CPV) for data-driven analysis of our legacy pharmaceutical products. Utilizing data management systems and statistical tools, you will evaluate process capabilities and initiate improvement strategies benefiting our solida and liquida products.

**Who You Are**:

- You hold a graduate degree (or equivalent) in engineering, life sciences, or pharmacy, providing a solid understanding of relevant theories, principles, and concepts.
- You possess extensive professional experience of 4-9 years in a similar role.
- You have in-depth knowledge of project management, process optimization, product development, Good Manufacturing Practices (GMP), and statistics (e.g. six sigma).
- You have experience leading and working in cross-functional teams.
- You demonstrate strong oral and written communication skills in both English and German.

**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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