Senior Research Scientist
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Would you like to be part of a team that plays a significant role in the innovative pipeline of creating new medications through the implementation of advances technologies? Do you love, and live for immunoassays? Do you thrive with handling and completing diverse tasks for numerous projects under restricted timelines? Then you are on the right path to become our new colleague. We are looking for a Senior Research Scientist or Research Scientist (depending on experience). Apply now! The position The position has focus on binding assays, both traditional ELISA and analytical techniques such as Surface Plasmon Resonance (SPR) and Bio-layer interferometry (BLI) along with SDS-Page and Western blot. The position is a balanced mix of analytical assay development, assay validation and support of the project process development. Your core responsibilities will be to: Develop and implement relevant assays for early state projects in a Chemistry, Manufacturing and Control (CMC) analytical department
Validate the assays and equipment to the appropriate level
Secure a smooth transfer of our methods to Product Supply (PS) when the project reaches clinical phase 3
Prepare documentation reports, change requests and deviations
Work across teams in our department
Participate in cross organizational project groups, collaboration with other departments both in Research Units and in manufacturing (Product Supply)
Combine hands-on experience from the immunoassay world with modern aspects such as automation.
As part of your role, you will initiate contact with relevant internal or external stakeholders to secure the best possible scientific cooperation and results across functions and teams. There will be a close day to day cooperation with our laboratory technicians and colleague scientist, thus we welcome and encourage you to perform laboratory work. You can look forward to using your skills and talent not only in our department but across Drug Development which covers analysis, cell banking, drug product development and stability testing from the R&D clinical portfolio to the supply chain. Qualifications To excel in this role you: Hold a Master of Science and/or a PhD within pharmacy, biomedicine, or similar, ideally combined with relevant experience with immunoassays e.g., ELISA from the pharmaceutical industry or similar.
Have interest in and preferably experience in working with Lab automation
Are a frontrunner when it comes to digitalization and automation.
Are eager to see things moving forward in a dynamic environment where projects vary, and thereby demands the need for flexibility and skills to organise and drive tasks.
Possess a good understanding of the drug manufacturing process
It will be an advantage if you have: Experience with communicating with regulatory authorities and preferable a QC-mindset
Have been working in a cGMP environment and take a pragmatic approach to problem solving and have a strong quality mindset.
You are a proactive team player, building relationships effortlessly. Your independence drives initiatives, meets deadlines, and handles multiple tasks without losing sight of the end goal. With excellent communication skills, a positive mindset, and a good sense of humour, you bring a well-rounded approach to your role. About the Department CMC (Chemistry Manufacturing and Controls) 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. Within the department we develop bioanalyses for analysis of cell banks, in-process samples, drug substance, and drug product samples for the entire Novo Nordisk project portfolio from early research to clinical trials all over the world. In our team, we develop immunoassays for monitoring of process related impurities and in-vitro potency of drug candidates, and support process development. You will join a team of 16 highly skilled scientists and laboratory technicians who work closely together with the rest of the department on projects to deliver on time at the right quality. 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 e-mail Associate Manager Christina Wiid Svarrer at [email protected] Deadline 11 August 2023. Applications will be considered on a continuous basis. 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 "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 10.7.2023, 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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