Analytical Op&QC Planner
vor 2 Monaten
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.
We are leading global biopharmaceutical company known for its innovative research and development. The new Building in Corsier-sur-Vevey is dedicated to advancing scientific and operational excellence in biopharmaceutical production. We aim to foster a culture of innovation, efficiency, and sustainability.
We are seeking a highly organized Quality Control Planner to join our QC team. The QC Planner will be responsible for developing and managing detailed schedules for all QC laboratory activities, ensuring efficient workflow and adherence to high-level planning timelines.
Your Role:
- Develop and maintain detailed schedules for all QC activities, including sample testing, equipment calibration, and maintenance
- Work closely with QC analysts and managers to forecast activity volumes and plan resources accordingly
- Monitor and report on schedule adherence and adjust to ensure alignment with high-level project timelines
- Collaborate with cross-functional teams, including production, supply chain, and project management, to integrate QC planning with overall site operations
- Participate in strategic planning meetings to align QC activities with broader site goals and initiatives
- Implement and maintain planning tools and systems to enhance visibility and tracking of QC activities
- Identify and address potential bottlenecks or delays in QC processes and propose solutions to optimize workflow
- Ensure compliance with all regulatory requirements, company policies, and safety standards
Who you are:
- Bachelor's degree in science, Business Administration, or related field
- Minimum of 2 years of experience in planning or scheduling in a laboratory or manufacturing environment, preferably in the pharmaceutical or biotech industry
- Strong understanding of QC processes and regulatory requirements in a GMP environment
- Proficient in MS Office and planning software (e.g., Microsoft Project, SAP, BINOCS, GLIMS)
- Excellent organizational, communication, and analytical skills
- Fluent in English; proficiency in French is a plus
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
Apply now and become a part of our diverse team
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