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.
Your Role:
The role involves ensuring that duties are conducted in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). This includes reviewing and approving various GxP documents such as protocols, technical specifications, batch records, and standard operating procedures (SOPs). Additionally, the position entails auditing and approving manufacturing or testing documentation to ensure compliance with regulatory standards and approved procedures. Collaboration with other departments to ensure internal procedures are followed, conducting internal audits as needed, participating in projects, supporting the maintenance of quality management systems, and reviewing and closing events are also key responsibilities.
Who You Are:
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!