Senior Downstream Scientist
- Category:
- Manufacturing
Are you a motivated professional who excels in solving complex process challenges and guiding your colleagues through systematic problem-solving? Do you bring a strong interest and experience in downstream processes, eager to work at the bridge of development and manufacturing? If you are ready to play a key role in optimizing and ensuring consistent production of our Active Pharmaceutical Ingredients (API), we are looking for two new colleagues to join us in API Manufacturing Science and Technology (MSAT) Downstream Process Support. Apply today! The position As one of our Senior Downstream Scientists, you will get a unique chance to work at the crossroad between development and GMP manufacturing, supporting one of our API production factories – either for Haemophilia & other Rare Diseases or Diabetes & Obesity products. You will work closely with members of your team, other teams in MSAT, manufacturing sites, and stakeholders in the product project teams to coordinate the relevant deliveries across the organization. You will provide active scientific support for our API production sites in Gentofte, Hillerød, Kalundborg, Clayton (US), and New Hampshire (US). Your key tasks will include:
- Developing and maintaining core documentation processes and control strategies related to API master formulas, in-process controls, risk assessments, and drug substance quality specifications
- Providing scientific support for troubleshooting, improvements, expansions, and optimisation for the API production sites
- Ensuring compliance with regulatory requirements and confidently addressing inquiries from authorities to uphold quality standards
- Setting-up yield, process optimisation, and experiments in our in-house laboratory
- Collaborating closely with production, QA, development, Regulatory Affairs, analytical departments, and project department
- Hold a PhD in chemical engineering, biotechnology, chemistry, or a related field, coupled with relevant industry experience, OR alternatively,
- Have a master’s degree with a minimum of 3 years of practical experience in a GMP environment within the pharmaceutical, biotechnology, or food production sectors
- Bring solid expertise in downstream purification processes
- Demonstrate strong communication and collaboration skills to ensure efficient distribution of tasks and alignment across the team
- Display full professional proficiency in both oral and written English
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.