Senior Scientist for Dose Formulation Analysis
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Are you a highly qualified and motivated Senior Scientist within development and validation of analytical methods? Do you have experience with Dose Formulation Analysis (DFA)? And are you ready to take on the responsibility of coordinating the outsourced activities to different contract research organizations (CROs) in non-clinical studies performed around the globe? If yes, then this opportunity might be right for you, so apply today! The position 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. You will hold a cross-functional collaboration and coordination role in the non-clinical projects. To ensure smooth collaboration and timely delivery of data, you will regularly communicate and conduct meetings with CRO’s. In addition, your responsibilities will be: Act as a Scientific monitor for DFA in non-clinical studies.
Review and approve study plans and reports.
Ensure the right level of science and quality GLP.
Facilitate method development/transfer and validation of HPLC-UV methods for dose formulation analysis.
Contract the above activities.
Qualifications You hold a Master´s in Life Sciences and have preferably a minimum of 3 years of experience with development and validation of analytical methods. You have strong written and oral communication skills in English as well as the capability to work in an interdisciplinary environment. Preferably, you are: Experienced with dose formulation analysis or analysis of formulated pharmaceuticals.
Familiar with GLP regulations and EMA/FDA/OECD guidelines.
Have a quality mindset, e.g., have experience as a Principal Investigator or Study Director for GLP studies.
Experienced in collaborating with external laboratories.
Talented in organising and creating overview in an ever-changing environment.
You are flexible, ambitious, focused on results 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 will join a team in a highly dynamic and challenging environment within the DFA team. About the department The Department of Non-clinical and clinical Assay sciences is responsible for DFA as well as bioanalysis in non-clinical 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 department is part of the Global Drug Discovery in Novo Nordisk A/S. The group supporting DFA currently consists of 3 scientists, and you will be organised in the LCMS Bioanalysis department which currently employs 21 people (9 laboratory technicians and 12 scientists). Working at Novo Nordisk
At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes and obesity. 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. Contact For further information, please contact Sune Hove Sporring at+4530794905. Deadline 18 June 2023Please 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 to 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.
At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes and obesity. 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. Contact For further information, please contact Sune Hove Sporring at+4530794905. Deadline 18 June 2023Please 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 to 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 1.6.2023, 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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