Senior Scientist for CMC Analytical Support

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Måløv

Senior Scientist for CMC Analytical Support We are seeking a highly qualified, motivated and energetic Senior Research Scientist for a position in CMC Analytical Support to drive and support our work in structural characterization of peptides, proteins and oligonucleotides. About the department CMC Analytical Support consists of 70 highly skilled colleagues divided in four analytical teams supporting the development organisation with expertise in specialized analytical tasks from late discovery to product launch. Our product pipeline is expanding, and you will have ample opportunities to be part of an innovative and interesting future. The department is part of Chemistry Manufacturing Control Development (CMC Development), located in Måløv. The department is responsible for peptide, protein and oligonucleotide characterisation including particle characterisation and stability studies. Furthermore, we are responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substance, drug product and side chains as well as for raw materials, excipients, and various process related residues and leachables. Providing analytical support to all parts of Novo Nordisk, the department acts as a link between the research units and product manufacturing, spanning from early development to phase 3 clinical trials and registration. As part of Novo Nordisk, CMC Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture, and distribute drug candidates for non-clinical and clinical trials and represent a strong culture with a “can do” mind-set.
The position You will be part of team “Peptide & Protein Characterization”, responsible for elucidation of structure and characterization of impurities of peptides, proteins and oligonucleotides. The team consists of 8 scientists and 7 technicians – all experienced, dedicated, and with a “can-do” attitude and we are seeking a highly qualified, engaged and energetic Senior Scientist.
Your primary responsibilities will include:
  • Planning, performing and coordinating structural characterisation input to development projects. This could consist of verification of the primary structure of an API batch, identification of impurities or providing scientific ad hoc support on a specific challenge.

  • In project teams you will collaborate closely with stakeholders and colleagues from across the organisation and design, interpret and report experiments - hereby generating pharmaceutical documentation for internal and external use.

  • Work closely together with lab techs to solve issues at hand and will, when needed, go to the lab and execute experiments.

  • Aid in bringing new technology / instruments to the lab and get it implemented in our workflow.

  • Qualifications The optimal candidate holds a PhD in chemical engineering, pharmaceutical science, biochemistry, or another relevant scientific discipline combined with:
  • a minimum of 3-5 years hands-on experience with structural characterisation and analysis of peptides, proteins and/or oligonucleotide and smaller biomolecules by LC-MS.

  • a solid understanding of organic synthesis and reaction mechanisms.

  • It is an advantage, if you also have:
  • experience from the pharmaceutical industry and knowledge of pharmaceutical development processes as well as experience with writing documents for regulatory use and knowledge of GMP.

  • programming and mathematic modelling skills.

  • Automation- and optimisation experience.

  • Solution state NMR experience within peptides/oligonucleotides and proteins.

  • On a personal level, you work systematically and meet your deadlines, have good communication- and collaborative skills and you are used to adhering to strict documentation standards for your work. We expect you to be out-going, to show business understanding, thrive in a performance culture and ability to take ownership of complex tasks. We also appreciate a can-do-attitude and ability to adapt to new situations. Contact
    For further information, please contact team leader Jonas Jensen at +45 3448 0391 or specialist Brian Kristensen at +45 3075 1173.

    Deadline
    10th of June 2023, however applications are evaluated continuously, so please apply as soon as possible. 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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".

    Arbejdsstedet er beliggende i Måløv.

    Jobbet er oprettet på vores service den 17.5.2023, 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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