Mos Compliance Associate Manager

vor 3 Wochen

CorsiersurVevey, Schweiz Merck KGaA 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**:

- Manage and develop your team to ensure a lean organization and achieve service and company objectives
- Provide guidance on routine compliance activities and oversight on team’s deliverables to ensure adequacy with quality standards and efficiency objetives
- Proactively identify potential gaps, propose and implement efficient CAPA to improve quality of operation
- Provide leadership and expertise on troubleshooting, investigation, continuous improvement initiatives/projects as well as during inspections
- Dispense trainings to manufacturing personnel, develop and share good practices
- Define and pilot key quality indicators for production department and ensure efficient governance
- Ensure a strong client orientation within production suites
- Be the central contact point regarding compliance topics and questions. Represent Production department in relevant committees (e.g. quality council, steering committee) and ensure strong cross-functional collaboration.

**Who you are**:

- Bachelor/Master degree with at least 5 years of experience within a biotech/pharmaceutical GMP environment (manufacturing, quality assurance or technical support functions)
- Excellent leadership and people management skills
- Strong knowledge of compliance requirement (regulations, guidelines, regulatory audits) in manufacturing industry along with understanding of quality management systems
- Strong analytical and problem-solving skills
- Adaptability: ability to handle competing priorities in a fast-pacing environment, emphasizing achieving results, resilience and proactive approach to compliance and quality
- Effective communication, stakeholders management and promotion of a quality culture
- Fluency French and excellent command of English (fluency is an asset)

**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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