The Bacterial Vaccine department is recruiting a Senior associate/associate  scientist – Biophysical characterization (Ph.D. or M.Sc. with equivalent experience) for two major vaccine projects. This position is a contractor job linked to a long-term project requirement. Based on outstanding results and positive feedbacks, the transition to an appropriate Janssen position is planned for this position. In your work, you will interact with various Bacterial Vaccines teams and with Janssen vaccine support departments. In addition, you will be expected to perform laboratory work in person (core part of the job) and help contract research organizations plan and execute their assignments. 
 
The Bacterial Vaccines department is strengthening its biophysical assay capabilities centered mainly on multidomain proteins and glycoprotein antigens. This position has, therefore, a strong focus on the biophysical characterization of large molecules. 
 
Your primary responsibilities will be:

•  Analyze protein-, or glycoprotein-based antigens (focus methods: DLS, microDSC, nano DSF & FTIR)
• Know, implement, and improve established tests for adjuvants, proteins, glycoconjugates, and particle-based vaccines.
• Support equipment selection, purchase, and maintenance for the BacVac AD facility.
• Be part of a team of two-three technicians and actively engage in the weekly resource planning of the BacVac AD team
• Perform and implement pre-formulation experiments and analyses related to the biophysical characterization of large molecules, specifically proteins, glycoproteins, and/or peptides.
• Apply state of–the art analytical chemistry to ensure a targeted approach to problem-solving and delivering relevant results. Work in a multidisciplinary team of researchers and show a willingness to learn/explore new techniques.
• Act quickly and provide expertise and solutions for advanced characterization of pharmaceutical products and support investigations. Develop test procedures and write scientific and study reports
• Ensure compliance with regulatory requirements, GMP, and safety.
• You will be reporting to a senior scientist
• Support CROs to plan, execute, document, and review their work.