QA Manager for Manufacturing Development
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Bagsværd
Do you want to make a difference within leadership and take on the responsibility of an experienced QA (Quality Assurance) team? Are you motivated by setting a clear direction and inspire your colleagues to produce great results? Are you ready to take the next step in your career and help us make a change for millions of people living with diabetes worldwide? Then this might be the right opportunity for you, apply today!
The position
As a Manager in IFP (Injected Finished Products) QA for Manufacturing Development, you will be responsible for a team of skilled and experienced QA professionals and specialists and report directly to the director.
Your key responsibilities will include:
• Motivating, leading, empower and setting directions for your team members
• Supporting your team members in complex cases
• Ensuring skills and competencies in the team are in place
• Building and maintaining strong collaborations with our stakeholders
• Keeping the processes simple and continuously striving for improvements
You will be growing personally and professionally by developing your leadership competencies and responding to exciting challenges with a high impact on the results for both the CVP area as well as the entire IFP. Our working environment is flexible, dynamic, and informal with a strong culture of cross-functional collaboration.
Qualifications
To succeed in this position, you:
• Hold a master’s degree in pharmacy or biotechnology or other nature science based relevant fields
• Have acquired experience from a pharmaceutical industry and project or people management positions
• Preferable have experience within production processes and/or QC/laboratory
• Have a strong quality mindset, well-developed business sense and problem-solving skills
• Communicate fluently in English, and preferably Danish
We are looking for a visible leader who can see the big picture and proactively strives for higher levels of performance. Furthermore, you are structured and well organized and create strong results by engaging your employees in taking pride in delivering on their objectives and individual development.
About the department
IFP Manufacturing Development is a support function to IFP, supporting all processes and products within it. IFP QA Manufacturing Development is the quality department which ensures that quality is incorporated in all aspects.
Our department consists of 48 highly qualified employees divided into teams of QC, Products & Processes, and Support. We are responsible for assuring quality and compliance of QC laboratories and Manufacturing Development activities for IFP production sites across the world as well as performing project management for cross-organizational projects, driving digitalization in IFP QA, and supporting with audits and inspections.
You will be a part of a department that works in a vibrant and positive working environment and values the exchange of knowledge and experience. Networking, high level of knowledge and cooperation are key to our success.
Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our careers is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 50.000 employees. Together, we go further. Together, we’re life-changing.
Contact
For further information, please contact Director Ea Pettersson +
Deadline
5 April 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 to your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At 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
As a Manager in IFP (Injected Finished Products) QA for Manufacturing Development, you will be responsible for a team of skilled and experienced QA professionals and specialists and report directly to the director.
Your key responsibilities will include:
• Motivating, leading, empower and setting directions for your team members
• Supporting your team members in complex cases
• Ensuring skills and competencies in the team are in place
• Building and maintaining strong collaborations with our stakeholders
• Keeping the processes simple and continuously striving for improvements
You will be growing personally and professionally by developing your leadership competencies and responding to exciting challenges with a high impact on the results for both the CVP area as well as the entire IFP. Our working environment is flexible, dynamic, and informal with a strong culture of cross-functional collaboration.
Qualifications
To succeed in this position, you:
• Hold a master’s degree in pharmacy or biotechnology or other nature science based relevant fields
• Have acquired experience from a pharmaceutical industry and project or people management positions
• Preferable have experience within production processes and/or QC/laboratory
• Have a strong quality mindset, well-developed business sense and problem-solving skills
• Communicate fluently in English, and preferably Danish
We are looking for a visible leader who can see the big picture and proactively strives for higher levels of performance. Furthermore, you are structured and well organized and create strong results by engaging your employees in taking pride in delivering on their objectives and individual development.
About the department
IFP Manufacturing Development is a support function to IFP, supporting all processes and products within it. IFP QA Manufacturing Development is the quality department which ensures that quality is incorporated in all aspects.
Our department consists of 48 highly qualified employees divided into teams of QC, Products & Processes, and Support. We are responsible for assuring quality and compliance of QC laboratories and Manufacturing Development activities for IFP production sites across the world as well as performing project management for cross-organizational projects, driving digitalization in IFP QA, and supporting with audits and inspections.
You will be a part of a department that works in a vibrant and positive working environment and values the exchange of knowledge and experience. Networking, high level of knowledge and cooperation are key to our success.
Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our careers is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 50.000 employees. Together, we go further. Together, we’re life-changing.
Contact
For further information, please contact Director Ea Pettersson +
Deadline
5 April 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 to your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At 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 Bagsværd.
Jobbet er oprettet på vores service den 22.3.2024, 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.
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