Global Label Expert - Regulatory Compliance (full-time / part-time) in Darmstadt bei Merck KGaA

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:

“Translating strategy into action” is our motto. As a Global Label Expert (all genders), you are responsible to develop and implement labelling strategies to comply with regulatory requirements across different jurisdictions. Above all, you will stay updated with global regulations, identify, and mitigate labelling-related compliance risks, working collaboratively within cross-functional teams to implement corrective actions. You are establishing and maintaining global label SOPs, deliver regulatory training programs and best practices to internal teams. Additionally, you will monitor industry forums and participate in relevant conferences/events to stay informed about emerging trends, regulations, and best practices in labelling. As GLM is part of the Digital Transformation and hazard communication department of our company, you will be given the opportunity to bring your own digital ideas and exchange with our digital and data science community.

Who You Are:

• Bachelor or Master degree in Life Sciences or related discipline

• 2+ years of experience in IVD, medical device (MD) or chemical industry

• Strong knowledge of label related regulations and quality standards within IVD, MD and chemistry, including CLP, IVDR, MDR, ISO standards

• Comfortable working in complex environments within multi-cultural and multidisciplinary teams

• Excellent communication and project management skills with the ability to effectively communicate complex regulatory requirements to cross-functional teams and key stakeholders

• Very good knowledge of English, good knowledge of German is a plus

• Knowledge in Label design software and ERP (SAP EHS) are 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!