Adv Development Scientist for CMC Virus Safety team

Cari; København; Híbrido; DKK 570.000 - 838.000; Jornada completa

Descripción de la vacante

Novo Nordisk in Gentofte seeks an Advanced Development Scientist to lead virus safety strategies within the CMC Virus Safety team. You will plan, execute and analyze downscaled purification experiments to develop robust virus clearance for Drug Substance projects, while advising stakeholders across functions.

The role blends hands-on work with scientific advisory and project coordination, offering opportunities to deepen expertise and drive progress in virus safety across development programs.

Formación

• M.Sc. in chemical engineering, biochemistry or related field.
• Experience with downstream purification steps (chromatography, filtration).
• Strong communication and cross-functional collaboration skills.

Responsabilidades

• Plan and conduct virus clearance evaluation studies via downscaled processes.
• Report experimental work and provide data to purification development.
• Coordinate virus safety activities for mammalian-expressed products.
• Collaborate with technicians and contribute to scientific writing.

Conocimientos

Downstream purification

Chromatography

Filtration

Stakeholder communication

Project coordination

Educación

M.Sc. in chemical engineering or related discipline

Herramientas

ÄKTA system

Descripción del empleo

Adv Development Scientist For CMC Virus Safety Team

Advanced Development Scientist

CMC Drug Development

CMC DS Process Operations, Virus Safety

Location: Gentofte

Your impact begins here

Are you experienced in virology and downstream purification, and motivated your expertise to virus safety? Join our CMC Virus Safety team, where you will take independent ownership, quickly build new knowledge and combine hands-on experimental work with scientific advisory and project coordination. Help shape the virus safety strategies behind tomorrow’s therapeutic products.

What you’ll do

As an Advanced Development Scientist in the Virus Safety team, you will work with experts across the Chemistry, Manufacturing & Control (CMC) Drug Development organisation to develop and manage virus safety strategies for Drug Substance projects. You will advise stakeholders, contribute to cross-disciplinary project teams and coordinate activities that ensure the virus safety of mammalian-expressed products in development.

A central part of the role is planning, executing and analysing downscaled downstream purification experiments. Your work will support the development of robust purification processes that remove and/or inactivate viruses. The position also provides strong opportunities to develop your scientific expertise and project management capabilities.

Your key responsibilities

• Plan and conduct virus clearance evaluation studies using downscaled purification processes.
• Plan, evaluate and report experimental laboratory work.
• Provide data and scientific input to purification process development.
• Collaborate closely with laboratory technicians, including troubleshooting technical issues and ensuring the delivery of high-quality project results.
• Contribute to scientific writing, including documentation for clinical trial applications.
• Coordinate virus safety activities for mammalian-expressed products in development.

What you’ll bring

To succeed in this role, we expect that you hold at least an M.Sc. in chemical engineering, biochemistry or another relevant discipline. You also bring:

• Have experience with downstream purification process steps, such as chromatography and filtration, for example using an ÄKTA chromatography system.
• Communicate effectively and collaborate confidently with stakeholders across functions and organisational areas.

It would be an advantage if you also have

• Relevant industry experience or a PhD.
• Experience from a GMP-regulated area.
• Knowledge of molecular detection techniques such as qPCR or RT-qPCR.

As a person, you are proactive, self-driven and comfortable taking independent ownership of your work. You learn quickly, seek out the knowledge needed to move tasks forward and apply new insights in practice. With a practical and solution-oriented mindset, you stay focused and adapt effectively when priorities or challenges change. You also enjoy collaborating, sharing knowledge and contributing to strong results with colleagues and stakeholders across the organisation.

Who you’ll work with

The Virus Safety team is part of the CMC Development organisation, which brings new therapeutic products into clinical trials. Based at our Gentofte site, the team assures the viral safety of API processes and biopharmaceutical products.

Our work is grounded in a strong scientific approach and carried out in multidisciplinary project groups. We collaborate closely with analytical and process development colleagues as well as international production facilities. The environment is dynamic and fast-changing, making curiosity, adaptability and a can-do attitude essential.

What you can expect here

At Novo, you can expect a role where your scientific judgement matters, your ideas are listened to, and your work helps move complex development projects forward. You will have opportunities to deepen your expertise, build cross-functional influence and grow in a collaborative environment where initiative is encouraged.

You will be supported to perform at your best and trusted to take ownership, while contributing to work that helps create progress for people living with serious chronic diseases.

Salary

Annual Base Salary ranges from DKK 570,200 to 838,100, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.

Incentives and Benefits

The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks. Learn more about our Reward Philosophy here.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.