Raw Material Scientist
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Måløv
Are you passionate about raw materials for tablets, i.e., Active Pharmaceutical Ingredients and pharmaceutical excipients, and do you understand how they impact the manufacturing process performance and drug product quality? Do you have experience with setting specification requirements and managing quality changes? Do you want to be part of a dynamic department who among other exciting tasks holds the responsibility of bringing new oral products for the treatment of diabetes and obesity from development to market readiness? Then this might be the right position for you. Read more and apply to become our new Raw Materials Scientist! The position
In this job you will participate in the transfer of new products from R&D to the production sites in both Denmark and the United States, with special focus on the raw material characteristics and their impact on the performance and robustness of the tablet production. As we expand our product portfolio and our production sites, we are also expanding our use of raw materials and its suppliers. We, therefore, expect you to participate in the ongoing implementation of new grades and types of raw materials. This includes testing the raw materials in lab-scale and in full-scale production equipment and setting requirements for specifications towards suppliers. Furthermore, you will be involved in the development of test strategies and development of small-scale powder characterization methods to measure, e.g., powder flow and compaction properties, to increase our knowledge about our raw materials and their impact on the drug product process and quality. You will contribute to:
• Evaluate new grades and types of raw materials
• Life cycle management with focus on raw materials for tablet production
• Development and implementation of state-of-the art powder characterization to improve tablet production processes
• Project management by leading projects and tasks across the organization
• Update of internal and external documents with requirements, specifications, and justifications
• Problem-solving in relation to process and quality challenges When necessary, you will be driving root cause analysis and trouble-shooting sessions in cooperation with the production and analytical departments among other important stakeholders. Qualifications
To master this role, you will need to combine your process and drug product understanding with a good quality mindset for the finished product. You will also have to build relations with your colleagues in the Production, Quality Control, Quality Assurance and Regulatory Affairs areas. To succeed, you:
• Hold a M.Sc. within Science, Pharmacy, Chemistry, Engineering or similar • Have at least + 2 years of experience from the pharmaceutical industry or academia, e.g., product development, support, transfer, or process validation • Good Manufacturing Practice (GMP) knowledge
• Are fluent in English
• ideally possess a Project Management toolbox It will be seen as an advantage if you have previous experience with raw materials for oral formulation and tablet production, as well as Danish proficiency. On a personal level, you possess great collaboration skills, are structured, have a natural sense of priority and not afraid of setting the direction and make tough decisions. Ultimately, you see yourself as a team-player who enjoys cross-functional, cross-departmental and stakeholder collaboration. About the department
Product Development & Launch employs approximately 100 highly skilled and motivated employees with the missions to bring oral solid dosage forms from early development to market production, optimize the processes and products, support the production sites, document the stability for the products and build up the documentation for authorities for new products and for marketed products. The department consist of three process development teams, two process analytical technology (PAT) teams, and a stability and specification team.
What we do is an important part of Novo Nordisk; hence, we solve exciting and challenging tasks every day. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact Associate Manager Søren Vinter Søgaard at +45 34487751. Deadline
November 5.th. 2023 We will review the applications continuously and book interviews on an ongoing basis, so please do not hesitate to apply. 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.
In this job you will participate in the transfer of new products from R&D to the production sites in both Denmark and the United States, with special focus on the raw material characteristics and their impact on the performance and robustness of the tablet production. As we expand our product portfolio and our production sites, we are also expanding our use of raw materials and its suppliers. We, therefore, expect you to participate in the ongoing implementation of new grades and types of raw materials. This includes testing the raw materials in lab-scale and in full-scale production equipment and setting requirements for specifications towards suppliers. Furthermore, you will be involved in the development of test strategies and development of small-scale powder characterization methods to measure, e.g., powder flow and compaction properties, to increase our knowledge about our raw materials and their impact on the drug product process and quality. You will contribute to:
• Evaluate new grades and types of raw materials
• Life cycle management with focus on raw materials for tablet production
• Development and implementation of state-of-the art powder characterization to improve tablet production processes
• Project management by leading projects and tasks across the organization
• Update of internal and external documents with requirements, specifications, and justifications
• Problem-solving in relation to process and quality challenges When necessary, you will be driving root cause analysis and trouble-shooting sessions in cooperation with the production and analytical departments among other important stakeholders. Qualifications
To master this role, you will need to combine your process and drug product understanding with a good quality mindset for the finished product. You will also have to build relations with your colleagues in the Production, Quality Control, Quality Assurance and Regulatory Affairs areas. To succeed, you:
• Hold a M.Sc. within Science, Pharmacy, Chemistry, Engineering or similar • Have at least + 2 years of experience from the pharmaceutical industry or academia, e.g., product development, support, transfer, or process validation • Good Manufacturing Practice (GMP) knowledge
• Are fluent in English
• ideally possess a Project Management toolbox It will be seen as an advantage if you have previous experience with raw materials for oral formulation and tablet production, as well as Danish proficiency. On a personal level, you possess great collaboration skills, are structured, have a natural sense of priority and not afraid of setting the direction and make tough decisions. Ultimately, you see yourself as a team-player who enjoys cross-functional, cross-departmental and stakeholder collaboration. About the department
Product Development & Launch employs approximately 100 highly skilled and motivated employees with the missions to bring oral solid dosage forms from early development to market production, optimize the processes and products, support the production sites, document the stability for the products and build up the documentation for authorities for new products and for marketed products. The department consist of three process development teams, two process analytical technology (PAT) teams, and a stability and specification team.
What we do is an important part of Novo Nordisk; hence, we solve exciting and challenging tasks every day. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact Associate Manager Søren Vinter Søgaard at +45 34487751. Deadline
November 5.th. 2023 We will review the applications continuously and book interviews on an ongoing basis, so please do not hesitate to apply. 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 20.10.2023, 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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