Manufacturing Development Scientist
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Måløv
Do you want to be an expert within problem-solving for both technical and process challenges? Are you passionate about using data and science to find the best solutions? Do you love to set direction by using your experience in the tableting fields? If so, you might be the right fit to become our new Manufacturing Development Scientist, apply today and you can be part of a life-changing career!
The position
In Manufacturing Development (Mdev), the Life Cycle Management (LCM) team holds the process responsibility for tablet manufacturing and supports a broad and growing portfolio of solid dose products on the market within Hormone Replacement Therapy (HRT), diabetes and most recently, obesity. The portfolio is expanding rapidly into more markets and therapy areas ensuring we never have a boring day.
In this role, you will be on top of our global oral tablet production processes and will use your acquired scientific and expert knowledge to support, solve-problems and optimize the manufacturing processes. In time, you will use your expert knowledge to set direction on cross-functional projects and decisions.
In our current setup, your tasks will alternate between the following:
• Act as process owner providing problem-solving support to the production sites in our global network
• Drive cross-functional projects to develop and optimize the manufacturing process for products on the market
• Perform and drive development studies hands-on in the laboratory and in the MDev production facilities
• Maintain documents describing the manufacturing process
• Prepare quality statements, rationales and manage changes to the process We strongly believe in a very thorough on-boarding, that will bring you closer to be a success in the role. Besides that, we encourage all our employee to take responsibility, together with us, for their professional and personal development.
As an employee in the LCM team, you will be able to take up a lot of responsibility and gain support to develop. You can expect to grow both on a personal and professional level. You will see - and experience your leader with a positive and agile mindset, to embrace change and adjustment to improve processes and quality for the future demands. Qualification As a MDev Scientist, you will need to combine your process and drug product understanding with a good quality mindset while also have solid stakeholder management skills to be able to collaborate with colleagues in the production, Quality Control, Quality Assurance and Regulatory Affairs areas. You will be the person driving collaboration in an ever-changing environment with quality and regulatory-related perspectives for the drug product.
To succeed in this role, you:
• hold a master’s degree in science within Pharmacy, Chemistry, Engineering, or similar
• have experience within the field of Chemistry, Manufacturing and Control or manufacturing, e.g., process or product support, transfer, or process validation
• are familiar with the project management toolbox
• possess good communication skills in both oral and written English and preferably also Danish
• As a person, you are a team player – open-minded, engaged, and able to inspire and motivate your colleagues. About the department
Oral Finished Products (OFP) MDev Support and Stability employs approximately 65 highly skilled and motivated employees with the missions to bring products from late 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 3 teams: Drug Product & Stability, LCM and New Product Entry. What we do is an important part of Novo Nordisk, and as an agile department, 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, Sara Cockerton at [email protected]. Deadline
16 April 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 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.
The position
In Manufacturing Development (Mdev), the Life Cycle Management (LCM) team holds the process responsibility for tablet manufacturing and supports a broad and growing portfolio of solid dose products on the market within Hormone Replacement Therapy (HRT), diabetes and most recently, obesity. The portfolio is expanding rapidly into more markets and therapy areas ensuring we never have a boring day.
In this role, you will be on top of our global oral tablet production processes and will use your acquired scientific and expert knowledge to support, solve-problems and optimize the manufacturing processes. In time, you will use your expert knowledge to set direction on cross-functional projects and decisions.
In our current setup, your tasks will alternate between the following:
• Act as process owner providing problem-solving support to the production sites in our global network
• Drive cross-functional projects to develop and optimize the manufacturing process for products on the market
• Perform and drive development studies hands-on in the laboratory and in the MDev production facilities
• Maintain documents describing the manufacturing process
• Prepare quality statements, rationales and manage changes to the process We strongly believe in a very thorough on-boarding, that will bring you closer to be a success in the role. Besides that, we encourage all our employee to take responsibility, together with us, for their professional and personal development.
As an employee in the LCM team, you will be able to take up a lot of responsibility and gain support to develop. You can expect to grow both on a personal and professional level. You will see - and experience your leader with a positive and agile mindset, to embrace change and adjustment to improve processes and quality for the future demands. Qualification As a MDev Scientist, you will need to combine your process and drug product understanding with a good quality mindset while also have solid stakeholder management skills to be able to collaborate with colleagues in the production, Quality Control, Quality Assurance and Regulatory Affairs areas. You will be the person driving collaboration in an ever-changing environment with quality and regulatory-related perspectives for the drug product.
To succeed in this role, you:
• hold a master’s degree in science within Pharmacy, Chemistry, Engineering, or similar
• have experience within the field of Chemistry, Manufacturing and Control or manufacturing, e.g., process or product support, transfer, or process validation
• are familiar with the project management toolbox
• possess good communication skills in both oral and written English and preferably also Danish
• As a person, you are a team player – open-minded, engaged, and able to inspire and motivate your colleagues. About the department
Oral Finished Products (OFP) MDev Support and Stability employs approximately 65 highly skilled and motivated employees with the missions to bring products from late 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 3 teams: Drug Product & Stability, LCM and New Product Entry. What we do is an important part of Novo Nordisk, and as an agile department, 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, Sara Cockerton at [email protected]. Deadline
16 April 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 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 5.1.2023, 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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