(Senior) Scientist for Dose Formulation Analysis
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Måløv
Are you skilled in coordination and thrive in collaborative team environments, ensuring timelines are met and deadlines are successfully achieved? If you have a background in Life Sciences, the Dose Formulation Analysis (DFA) team is eager to welcome you aboard! The position As a scientist in the DFA team, you will be responsible for outsourced DFA to support Good Laboratory Practice (GLP) compliant non-clinical safety and toxicology studies across all developing projects in the Novo Nordisk pipeline. Your responsibilities will include: Acting as a scientific monitor for DFA in GLP in vivo studies and other non-clinical studies Reviewing and approving study plans and reports from CRO’s Ensuring the right level of science and GLP quality in your daily work Facilitating method development/transfer and validation of HPLC-UV methods for dose formulation analysis Holding a cross-functional collaboration and coordination role in the non-clinical projects Regularly communicating and conducting meetings with CRO’s to ensure smooth collaboration and timely delivery of data Contracting the above activities Your tasks will require that you both submerge in scientific details and keep a general overview of all ongoing projects in the group. While the role doesn't involve hands-on laboratory work, your active participation and contribution of scientific expertise are crucial to supporting laboratory activities at CROs. Physical presence in Måløv is required, the job includes extensive interaction with internal stakeholders and other team members. The seniority level of the position will be dependent on your daily responsibilities, qualifications and experience. Qualifications You hold a Master´s degree in life sciences and have preferably minimum 3 years of experience working with HPLC-UV analytical methods or equivalent experience. Furthermore, you have the capability to work in a multidisciplinary environment. Preferably, you have several of the following skills: Experienced with dose formulation analysis or analysis of formulated pharmaceuticals (Drug Product) Have a quality mindset, e.g., have experience working within GxP regulated environment Experienced in collaborating with external laboratories Talented in organising and coordinating with external and internal parties Strong written and oral communication skills in English As a person, you are flexible, have strategic and investigational thinking, take pride in delivering on time and have a good sense of humour. You have a strong drive and are good at communicating and collaborating in cross-disciplinary teams and with external contributors. You are able to work in a highly dynamic and challenging environment. About the department The Department of Nonclinical and Clinical Assay Sciences is responsible for DFA as well as for bioanalysis and immunogenicity assessment in non-clinical in vivo studies and clinical trials. We cover the entire project portfolio at Novo Nordisk A/S. We are delivering according to Good Laboratory Practice (GLP). The group supporting DFA currently consists of 3 employees. The DFA team is responsible for analysis of doses in formulated drug products (DP) for use in GLP regulated in vivo studies. We work according to EMA, FDA, and OECD guidelines. We coordinate and outsource analytical studies of DP and validation studies to CROs and are in daily contact with many stakeholders to collect knowledge, project timelines, technical data, facilitate method transfer and support ongoing in vivo studies with our results. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Sune Hove Sporring, Director at +4530794905. Deadline 10 December 2023. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified. 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. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your 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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 23.11.2023, 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.
- Forretningsudvikler
- Måløv
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