Drug Product Scientist
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Måløv
Do you want to be part of a dynamic department that holds the product responsibility for oral products for hormone replacement therapy, diabetes and obesity? Do you have experience with documentation of solid dose drug products?
Apply now and become our new Drug Product Scientist!
The position
In the Lifecycle Management (LCM) Team, you will be primarily responsible for the Hormone Replacement Therapy (HRT) drug products. The LCM portfolio is growing and in the future you will also have the opportunity to work on other drugs in the portfolio within diabetes, obesity and other treatments.
Your primary tasks will be to:
• document and define the product quality of oral products
• data analysis, calculations and quality statements/rationales
• drive projects and changes with regulatory impact
• problem solving and support to QC, stability and production sites in our global network Further, you can be involved in different disciplines, including risk assessments, drug product strategies, regulatory documents and stability studies.
You will be the person driving collaboration in an ever-changing environment with many different stakeholders and your colleagues in the Stability team, Quality Control, Quality Assurance and Regulatory Affairs areas, discussing quality and regulatory-related concerns for the drug product. This will allow you to broaden you network across the organization.
We strongly believe in a very thorough onboarding, 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.
Qualifications
To succeed with all this, you will need a good drug product understanding with a good quality mindset.
We are looking for a candidate with the following background:
• You hold a master’s degree in science within Pharmacy, Chemistry, or a similar field
• 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 in time 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.
A bout the department
In Oral Finished Product (OFP) Manufacturing Development Support and Stability in Måløv we are about 65 engaged and open-minded colleagues organised in 3 teams: Stability, Lifecycle Management, New Product Entry (NPE). We are responsible for the specifications of OFP’s drug products and transfer of products from Chemistry, Manufacturing and Control to our production facilities in Product Supply and the support of our productions.
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 notice our positive and agile mindset, and our ability to embrace change and adjustment to improve processes and quality for the future demands.
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
28 May 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.
Apply now and become our new Drug Product Scientist!
The position
In the Lifecycle Management (LCM) Team, you will be primarily responsible for the Hormone Replacement Therapy (HRT) drug products. The LCM portfolio is growing and in the future you will also have the opportunity to work on other drugs in the portfolio within diabetes, obesity and other treatments.
Your primary tasks will be to:
• document and define the product quality of oral products
• data analysis, calculations and quality statements/rationales
• drive projects and changes with regulatory impact
• problem solving and support to QC, stability and production sites in our global network Further, you can be involved in different disciplines, including risk assessments, drug product strategies, regulatory documents and stability studies.
You will be the person driving collaboration in an ever-changing environment with many different stakeholders and your colleagues in the Stability team, Quality Control, Quality Assurance and Regulatory Affairs areas, discussing quality and regulatory-related concerns for the drug product. This will allow you to broaden you network across the organization.
We strongly believe in a very thorough onboarding, 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.
Qualifications
To succeed with all this, you will need a good drug product understanding with a good quality mindset.
We are looking for a candidate with the following background:
• You hold a master’s degree in science within Pharmacy, Chemistry, or a similar field
• 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 in time 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.
A bout the department
In Oral Finished Product (OFP) Manufacturing Development Support and Stability in Måløv we are about 65 engaged and open-minded colleagues organised in 3 teams: Stability, Lifecycle Management, New Product Entry (NPE). We are responsible for the specifications of OFP’s drug products and transfer of products from Chemistry, Manufacturing and Control to our production facilities in Product Supply and the support of our productions.
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 notice our positive and agile mindset, and our ability to embrace change and adjustment to improve processes and quality for the future demands.
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
28 May 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 4.5.2023, 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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