Analytical Coordinator
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Måløv
Would you like to be part of the journey where the near future holds an ambitious strategy for exciting new products? Do you want to set direction and coordinate the implementation and validation of new analytical methods in Quality Control (QC) and coordinate the required validation level at CMO’s (Contract Manufacturing Organizations)?
If so, then read more and apply to become our new Analytical Coordinator! About the department
In Oral Development & Finished Products (ODFP) QC we are approximately 200 dedicated employees in Måløv, and the area is still growing. For the future we have many ambitions - together we will succeed and still strive being at the forefront of the development of technology, systems, and processes etc. The strategy will not succeed itself, but our QC culture helps to ensure that we succeed together. We believe that “Everything Builds on People” and we aim to drive changes by being forward looking, curious, brave and a reliable partner. The ODFP area consist of three departments, and you will join New Product Entry (NPE) where we receive, develop and mature analytical methods for our new products. We make sure that the methods are robust, validated, and ready for operation. The position
As an Analytical Coordinator your primary tasks will include:
• Coordination responsibility for validation and transfer of analytical methods
• Implementation of analyses at our contract manufacture
• Setting different analytical strategies for the project
• Participation as Analytical Coordinator in internal and external project teams
This will give you a variety of challenges, and therefore strong cross-functional collaboration with your colleagues and stakeholders is essential. You will be part of a dedicated team where ideas, problems and solutions are discussed in an open and positive atmosphere. The team you will join in NPE consists of 2 additional Analytical Coordinators, 2 QC specialists, Project Managers, Validation chemists and Laboratory technicians.
The CMO collaboration is a new area in ODFP QC, and we therefore it will be beneficial for you to have knowledge of such collaborations to fulfill the role.
Qualifications
To be successful in this role, you:
• Hold a Master´s Degree in Chemistry, Pharmacy, Engineering, or another within natural sciences
• Have experience with validation of analytical methods within
• Ideally have a strong background within CMOs
• Have experience with GMP, ICH guideline and pharmacopoeia requirements
• Full English proficiency, and will be an advantage to have Danish proficiency as well
Experience within qualification of equipment will be beneficial.
As a person, you enjoy working in project groups and have a high level of energy to drive yourself and your colleagues forward to deliver on milestones. You work in a structured manner and find solutions that are robust and will ensure the correct quality level. Finally, you motivate your colleagues with a positive, diplomatic, and forthcoming attitude. Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information, please contact Trine Kantsø, Director in NPE QC at [email protected]
Deadline
28 May 2023
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 so, then read more and apply to become our new Analytical Coordinator! About the department
In Oral Development & Finished Products (ODFP) QC we are approximately 200 dedicated employees in Måløv, and the area is still growing. For the future we have many ambitions - together we will succeed and still strive being at the forefront of the development of technology, systems, and processes etc. The strategy will not succeed itself, but our QC culture helps to ensure that we succeed together. We believe that “Everything Builds on People” and we aim to drive changes by being forward looking, curious, brave and a reliable partner. The ODFP area consist of three departments, and you will join New Product Entry (NPE) where we receive, develop and mature analytical methods for our new products. We make sure that the methods are robust, validated, and ready for operation. The position
As an Analytical Coordinator your primary tasks will include:
• Coordination responsibility for validation and transfer of analytical methods
• Implementation of analyses at our contract manufacture
• Setting different analytical strategies for the project
• Participation as Analytical Coordinator in internal and external project teams
This will give you a variety of challenges, and therefore strong cross-functional collaboration with your colleagues and stakeholders is essential. You will be part of a dedicated team where ideas, problems and solutions are discussed in an open and positive atmosphere. The team you will join in NPE consists of 2 additional Analytical Coordinators, 2 QC specialists, Project Managers, Validation chemists and Laboratory technicians.
The CMO collaboration is a new area in ODFP QC, and we therefore it will be beneficial for you to have knowledge of such collaborations to fulfill the role.
Qualifications
To be successful in this role, you:
• Hold a Master´s Degree in Chemistry, Pharmacy, Engineering, or another within natural sciences
• Have experience with validation of analytical methods within
• Ideally have a strong background within CMOs
• Have experience with GMP, ICH guideline and pharmacopoeia requirements
• Full English proficiency, and will be an advantage to have Danish proficiency as well
Experience within qualification of equipment will be beneficial.
As a person, you enjoy working in project groups and have a high level of energy to drive yourself and your colleagues forward to deliver on milestones. You work in a structured manner and find solutions that are robust and will ensure the correct quality level. Finally, you motivate your colleagues with a positive, diplomatic, and forthcoming attitude. Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information, please contact Trine Kantsø, Director in NPE QC at [email protected]
Deadline
28 May 2023
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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