Drug Product & Stability Scientist
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Måløv
Do you want to be part of a new and dynamic department working with solid dose products and other emerging technologies? Do you find it interesting to work with technical demands for storing drugs? Do you have experience with documentation for drug products? Then you might be our new colleague in Manufacturing Development Life Cycle Management Support – in short MDev LCM Support. The job
In the LCM team, you will be primarily responsible for one or more of our products in a growing portfolio covering drugs within diabetes, obesity, and hormone replacement therapy. Your primary task will be to: • Prepare protocols and reports that document the quality of our products and their stability within the labelled shelf life
• Data analysis, calculations, and quality statements/rationales
• Calculation of drug specification limits
• Plan and initiate stability studies in close collaboration with your colleagues
• Drive projects and changes with regulatory impact Qualifications • You hold a degree in science within pharmacy, chemistry, engineering or similar
• You have knowledge within the pharmaceutical industry and is used to following GMP
• You have experience within the field of Chemistry, Manufacturing and Control, Manufacturing, QC or similar
• Experience within oral formulation and tablet production will be an advantage
• You possess good communication skills in both oral and written English and preferably also Danish As a person, you see new possible investigation avenues when results deviate from the expected outcome and do not compromise on quality while completing your tasks and move on to new challenges with energy and enthusiasm. You are a team player – open-minded, engaged, and able to inspire and motivate your colleagues, also through very strong stakeholder management skills. About our department
MDev LCM Support contains of approximate 30 dedicated employees divided into 2 teams. The main purpose of the department is support within product quality, stability, manufacturing process and regulatory documentation for the authorities for marketed products. We support solid-dose products from production sites in Denmark, USA, and Algeria. Our department is an important link in Novo Nordisk Emerging Technologies area, and we are growing rapidly while solving exciting and challenging tasks. About Novo Nordisk
At Novo Nordisk we excel in using our competences, dedication, and ambitions to help patients with diabetes. We offer the opportunity to be a part of a global company, where passion and commitment is met with the opportunity to develop both personally and professionally.
Contact
For further information please contact Pia Grubbe (e-mail [email protected]). Deadline
9 July 2023 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 you 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.
In the LCM team, you will be primarily responsible for one or more of our products in a growing portfolio covering drugs within diabetes, obesity, and hormone replacement therapy. Your primary task will be to: • Prepare protocols and reports that document the quality of our products and their stability within the labelled shelf life
• Data analysis, calculations, and quality statements/rationales
• Calculation of drug specification limits
• Plan and initiate stability studies in close collaboration with your colleagues
• Drive projects and changes with regulatory impact Qualifications • You hold a degree in science within pharmacy, chemistry, engineering or similar
• You have knowledge within the pharmaceutical industry and is used to following GMP
• You have experience within the field of Chemistry, Manufacturing and Control, Manufacturing, QC or similar
• Experience within oral formulation and tablet production will be an advantage
• You possess good communication skills in both oral and written English and preferably also Danish As a person, you see new possible investigation avenues when results deviate from the expected outcome and do not compromise on quality while completing your tasks and move on to new challenges with energy and enthusiasm. You are a team player – open-minded, engaged, and able to inspire and motivate your colleagues, also through very strong stakeholder management skills. About our department
MDev LCM Support contains of approximate 30 dedicated employees divided into 2 teams. The main purpose of the department is support within product quality, stability, manufacturing process and regulatory documentation for the authorities for marketed products. We support solid-dose products from production sites in Denmark, USA, and Algeria. Our department is an important link in Novo Nordisk Emerging Technologies area, and we are growing rapidly while solving exciting and challenging tasks. About Novo Nordisk
At Novo Nordisk we excel in using our competences, dedication, and ambitions to help patients with diabetes. We offer the opportunity to be a part of a global company, where passion and commitment is met with the opportunity to develop both personally and professionally.
Contact
For further information please contact Pia Grubbe (e-mail [email protected]). Deadline
9 July 2023 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 you 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 21.6.2023, 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.
- Øvrige
- Måløv
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