Principal Scientist, Bioanalytics

Work Your Magic with us! Start your next chapter and join EMD Serono.

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.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

In the New Biological Entities Drug Metabolism and Pharmacokinetics (NBE DMPK) department, the Principal Scientist role is a scientific and operational role in Research and Development (R&D). Our company is committed to bringing transformational medicines to patients, and you will collaborate in a matrixed environment with other passionate functional experts to deliver novel biotherapeutics. You will be responsible for the development and fit-for-purpose validation of bioanalytical methods to be applied in sample analysis for molecules in discovery and development phases. Your work will support the characterization of multiple molecules and modalities, including multi-specific NBEs, antibody-drug conjugates, antibody oligonucleotide conjugates (AOCs), and other biologics, from molecule design through preclinical and clinical phases, thus fulfilling internal and regulatory requirements. Representative technologies could include innovative immunochemical and ligand binding techniques such as ELISA, MSD-ECLA, Gyrolab, and others. Additional duties will include development of complex experimental study designs, interpretation of analytical data, good knowledge of immunogenicity, and technical report writing according to current company and industry standards. You will be responsible for ensuring timely delivery, with appropriate quality, of LBA bioanalytical deliverables (method development, qualification, and its application to in-vivo animal studies), and if needed, responsible for conducting/supervising critical reagent characterization. You will be able to recommend data decisions to the lab manager by providing solid results, findings and technical solutions to project issues/problems. You will be able to conduct scientific literature research to address complex technical issues and evaluate and implement potential new analytical strategies and technologies as needed. You may also be responsible for monitoring bioanalytical studies at contract research organizations (CROs).