Dynamic Development Scientist for Oral Protein Formulation

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Måløv

  • Research
  • Måløv

Are you passionate about formulation, process development and manufacturing of solid dosage forms? Are you eager to be part of Novo Nordisk major quest within oral formulation? Do you want to influence a department working with processes on the edge of the future? If yes, you are the scientist that we are looking for in Oral Pilot & Process Development.

About the department

As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (CMC) Development makes a real difference for patients with chronic diseases across the world. We develop manufacturing processes and manufacture all new oral products out of our research units in our pilot plants, ensuring that we bring best-in-class treatments to the market. Our ambition is to develop break-through products based on orally available versions of GLP-1 and other molecules.

In Oral Pilot & Process Development we are 80+ colleagues, organised in three teams. We are responsible for formulation, process development and manufacturing of oral protein products for preclinical and clinical trials. The department covers a broad and exciting range of process technologies for solid dosage forms. We also cover technical support, project management and execution related to qualification of equipment, utilities and facility.

The job

You will be responsible for development, formulation and manufacturing processes for new oral drug products and comparator products in collaboration with CMOs (Contract Manufacturing Organisations). In particular, you will:

  • Setup and challenge project plans and project activities within development and production.
  • coordinate project activities in close collaboration with the technical coordinators and line management.
  • review documentation (e.g. Protocols and reports for development studies and Master Batch Records for GMP manufacturing), and ensure that the documentation from the CMOs live up to current guidelines and industry standards.
  • support the CMOs in handling deviations and change requests in order to improve daily work processes and to secure oral products for clinical trials.

You will play a key role in supporting and advising the Contract Manufacturing Organisations (CMOs) that we collaborate with. For you to succeed, it is therefore crucial that you have strong stakeholder management skills as well as an ability to understand the cultural and technical challenges linked to collaboration with CMOs. Additionally, you can look forward to acquiring professional knowledge within completely new processes as you will represent the department in multi-disciplinary project groups, in which you work closely with experts from a wide range of areas.

Qualifications

You have a Master’s degree within Life Sciences (e.g. Pharmacy) or similar and 2-5 years of experience with the pharmaceutical industry. Preferably, you have experience with the formulation and process optimisation of Solid Dosage Forms e.g. within mixing, granulation, compression, capsule filling, coating or pharmaceutical-technical analyses. It would also be an advantage to have experience with outsourcing of process development activities.

On a personal level, you are a self-starter, you have a structured approach to your tasks and you have the ability to take responsibility and make the right decisions. You like working in a dynamic environment, where teamwork is at the top of the agenda. You are innovative, focused on results and quality – and ready to contribute to the next generation of innovative oral products. In this position, you will also need good collaboration skills and great communication skills in English and ideally also Danish or another Scandinavian language. Lastly, we expect you to be ready to embrace changes and to have a strong quality mind-set.

Contact

For further information please contact Tanni Leth Lundsager at +45 3079 8379 or Sandie Bøge Winther at +45 3079 7529.

Deadline

Interviews will be taking place continuously.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


Information og data

Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 27.3.2020, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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