New Product Scientist
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Måløv
Are you motivated by upscaling and transferring of processes from development to phase III production? Do you have good communication skills and can explain the ‘why’ in GMP procedures? Are you ready to take responsibility for keeping our clinical phase III tablet production running?
If yes, you might just be the one we are looking for, apply now!
The position
In this role, the focus is transfer of new product entries (NPE) from late phase development to phase III clinical production in our GMP facility. You will have the responsibility of participating in cross functional project teams and in development activities to gain a strong knowledge of the process prior to transfer of process to phase III GMP production. As part of the preparation for the phase III productions/campaigns you will have the responsibility of making the processes GMP ready and updating documents and Standard Operating Procedures together with motivated colleagues. You will support operators and technicians during production, perform problem solving, and secure the right quality of the product for our patients. Your main responsibilities will be to:
• Plan, coordinate, complete and report work
• Prepare documentation for projects and clinical production
• Data handling
• Work LEAN with continuous improvements and problem solving
• Optimizing processes while following GMP procedures
Qualifications
To be successful in the role as New Product Scientist, you:
• hold a Master’s in natural science, engineering or similar
• have experience within production in a pharmaceutical setting, preferably tablet production
• have extensive knowledge of GMP principles
• can explain complex matters in a simple way using your great communication skills
• preferably are familiar with LEAN principles
• are fully proficient in English and can conversate in Danish On a personal level you are curious, result-oriented, structured and you take pride in planning and driving tasks forward to meet deadlines. You are a team player that knows it takes hard work to reach success, and also can positively influence your colleagues by staying calm and keeping on overview even in times of challenges. About the department
Oral Product Development (OPDev) Clinical Operations is located in site Måløv. The area is responsible of producing tablets as well as new products. You will be a part of the campaign support team in ET OPDev Clinical Operations. In the department we optimize production making the processes ready for GMP in large scale production. We transfer processes from R&D to commercial production.
Contact
If you want to know more about the position, you are welcome to contact Associate Manager Charlotte Johnsson at +45 30759470
Deadline
11 March 2024 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.
If yes, you might just be the one we are looking for, apply now!
The position
In this role, the focus is transfer of new product entries (NPE) from late phase development to phase III clinical production in our GMP facility. You will have the responsibility of participating in cross functional project teams and in development activities to gain a strong knowledge of the process prior to transfer of process to phase III GMP production. As part of the preparation for the phase III productions/campaigns you will have the responsibility of making the processes GMP ready and updating documents and Standard Operating Procedures together with motivated colleagues. You will support operators and technicians during production, perform problem solving, and secure the right quality of the product for our patients. Your main responsibilities will be to:
• Plan, coordinate, complete and report work
• Prepare documentation for projects and clinical production
• Data handling
• Work LEAN with continuous improvements and problem solving
• Optimizing processes while following GMP procedures
Qualifications
To be successful in the role as New Product Scientist, you:
• hold a Master’s in natural science, engineering or similar
• have experience within production in a pharmaceutical setting, preferably tablet production
• have extensive knowledge of GMP principles
• can explain complex matters in a simple way using your great communication skills
• preferably are familiar with LEAN principles
• are fully proficient in English and can conversate in Danish On a personal level you are curious, result-oriented, structured and you take pride in planning and driving tasks forward to meet deadlines. You are a team player that knows it takes hard work to reach success, and also can positively influence your colleagues by staying calm and keeping on overview even in times of challenges. About the department
Oral Product Development (OPDev) Clinical Operations is located in site Måløv. The area is responsible of producing tablets as well as new products. You will be a part of the campaign support team in ET OPDev Clinical Operations. In the department we optimize production making the processes ready for GMP in large scale production. We transfer processes from R&D to commercial production.
Contact
If you want to know more about the position, you are welcome to contact Associate Manager Charlotte Johnsson at +45 30759470
Deadline
11 March 2024 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 12.1.2024, 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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