Pilot Scientist

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Does improving production processes and workflows in a GMP production of oral formulations for phase 1 & 2 clinical trials, excite you? Then you may be our new Pilot Scientist for our Oral Pilot Plant in Måløv! Read on to see if it could be for you - Apply today and start a life-changing career. The Position As Pilot Scientist, you become part of a team of academics and technicians that support all aspects of powder technologies production processes, from blending to compression. Your tasks will include:
  • Working closely with various professional groups in a fast-paced environment to ensure quick and stable delivery of clinical products while maintaining high quality.
  • Handling and document errors and communicate knowledge to colleagues in the team and production.
  • Assessing data, write documentation, perform systematic problem-solving, and participate in project work to drive optimizations and innovation.
  • Taking the initiative to solve production challenges and involve colleagues when necessary.
  • A typical day as Pilot Scientist You sit at your desk working on a challenge regarding the production: Tablets are fragile and compression of them is difficult. You systematically run simple statistical calculations and plot in data in your search for patterns that could confirm your hypothesis, when you receive a meeting invite for the next day. It is a project concerning use of a new equipment, and your input is needed. As you reply, the phone rings. It is a technician from production. There has been an incident, and you make your way to production. The incident concerns a registration in the process control system (PAS-X), you sit down with the technician and patiently guide her through the data. Later the same day, you will have to open an incident report. Someone comments about the performance of the tabletting equipment. You wonder if this could have affected the compressibility of the powder. Another technician stops you in the hallway with a concern about the compression process that is running tomorrow. You listen carefully, acknowledge the input, and ask curious questions to make sure you understand the viewpoint. You promise to follow up. Back at your desk, you focus your data analysis on the tabletting equipment, and decide to spar with a colleague from Equipment Support. Together, you decide to initiate a maintenance check of the tablet press. On your way back, you check in with your colleague, who works on improving the compression step. A design is taking shape that will make it easier for the technicians to run the process the next day. Before you leave the office that day, you make a short visit back to production to tell the good news. Qualifications To succeed in this role, you have:
  • An academical degree within natural sciences.
  • Fluency in oral and written English.
  • Experience from a production and/or GMP regulated environment is a plus.
  • To thrive in this role, you
  • Are curious by nature, and challenge existing beliefs and come up with a new, innovative approach.
  • Work independently and structured and keep calm in a dynamic and sometimes unpredictable environment where tasks and plans can change quickly.
  • Get energy from helping others, building relations to people, and contribute to a strong community in the department.
  • Have a sense of humour and contribute to a positive atmosphere and culture in a busy workplace.
  • Listen first, when faced with practical challenges and viewpoints of others, and you thrive on feedback and openness.
  • About the Department Our department is a Good Manufacturing Practice (GMP) production, that produces oral formulations for phase 1 & 2 clinical trials. We aim is to achieve increased capacity by establishing robust processes through use of innovative solutions, optimizations, and new production technologies, while maintaining a healthy and committed work environment with psychological safety for all employees. Our focus is on succeeding together, which fosters high commitment and well-being for everyone. We celebrate our successes both small and big - and one of our main focuses is bringing out the best in each other. Contact For further information, please contact Associate Manager Annette Midtgaard Hvilsom +45 3079 3461 Deadline
    Apply no later than January 7th 2024 Please note that we will be reviewing applications on an ongoing basis, and we encourage you to apply as soon as possible.
    You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV
    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.


    Information og data

    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Måløv.

    Jobbet er oprettet på vores service den 28.12.2023, men kan have været deaktiveret og genaktiveret igen.

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

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