QA Manager in Global Contract Manufacturing
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Could you envision yourself leading the charge in Quality Assurance within Contract Manufacturing Organizations (CMO) Drug Substance Operations? Are you ready to take on the challenge of driving leadership and fostering team development to meet the dynamic demands of the business? Picture the excitement of making impactful decisions on a global scale and shaping the future of excellence in external manufacturing. Join our company and embark on a life-changing career journey! The position
As a Manager in Global Contract Manufacturing Quality Assurance – Drug Substance (GCM QA DS), you will drive Quality Assurance for one of the two Operational teams. The team is responsible for QA oversight and batch release from our CMO’s in the commercial phase. Furthermore, the team take active part in the transfer from the project phase to the commercial phase. Collaboration between the two Operational teams and the project team is key to be successful. Your main responsibilities will be to: • Drive leadership & team development to ensure continuous team/people development to fulfil business demands
• Proactively manage QA resources to secure release of product from the CMO and to the right QA oversight at the CMO
• Ensure that our processes are continuously improved, some of the improvements that we are looking into are Digital batch release
• Proactively seek close collaboration with internal and external key stakeholders to ensure alignment on external requirements, QMS, business needs, and resources This role will give you high degree of ability to make independent decisions that will represent Novo Nordisk in an international context under sometimes challenging conditions due to cultural, national or political restrictions when operating. Due to the international nature of the job, you will have the opportunity to travel to CMO partners globally. Qualifications
The candidate we are looking for is able to manage both the quality requirements and business perspective, with an ability to balance quality, delivery and cost efficiency. To succeed in this role, you have: • Master’s degree in Pharmacy, Engineering, Biochemistry or similar
• Extensive experience in a GMP regulated manufacturing organization
• Solid experience within finished products or Quality Assurance
• Proven leadership experience
• Fluency in English, both written and spoken On a personal level, you proactively challenge problems, remove obstacles and take decisions to ensure execution, seeking influence and staying firm when needed to secure the quality and compliance aspects. Clear communication will be the key, as well as the ability to demonstrate authority but also trust. Your leadership style is collaborative and inclusive, and you have the ability to listen, coach and motivate employees to deliver their best – engaging them in taking pride when meeting their objectives. About the department
Currently, the area consists of 35 highly qualified employees in 3 different teams, but we are growing very fast and expecting to become bigger in the nearest future. We are working in an international environment with many different companies and stakeholders with engagement, trust, and mutual respect. Our performance is driven by the wish to think big, improve and simplify our way of working while ensuring quality compliance, product quality and patient safety. Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career 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. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Vice President, Trine Kantsø at +45-30794362 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.
As a Manager in Global Contract Manufacturing Quality Assurance – Drug Substance (GCM QA DS), you will drive Quality Assurance for one of the two Operational teams. The team is responsible for QA oversight and batch release from our CMO’s in the commercial phase. Furthermore, the team take active part in the transfer from the project phase to the commercial phase. Collaboration between the two Operational teams and the project team is key to be successful. Your main responsibilities will be to: • Drive leadership & team development to ensure continuous team/people development to fulfil business demands
• Proactively manage QA resources to secure release of product from the CMO and to the right QA oversight at the CMO
• Ensure that our processes are continuously improved, some of the improvements that we are looking into are Digital batch release
• Proactively seek close collaboration with internal and external key stakeholders to ensure alignment on external requirements, QMS, business needs, and resources This role will give you high degree of ability to make independent decisions that will represent Novo Nordisk in an international context under sometimes challenging conditions due to cultural, national or political restrictions when operating. Due to the international nature of the job, you will have the opportunity to travel to CMO partners globally. Qualifications
The candidate we are looking for is able to manage both the quality requirements and business perspective, with an ability to balance quality, delivery and cost efficiency. To succeed in this role, you have: • Master’s degree in Pharmacy, Engineering, Biochemistry or similar
• Extensive experience in a GMP regulated manufacturing organization
• Solid experience within finished products or Quality Assurance
• Proven leadership experience
• Fluency in English, both written and spoken On a personal level, you proactively challenge problems, remove obstacles and take decisions to ensure execution, seeking influence and staying firm when needed to secure the quality and compliance aspects. Clear communication will be the key, as well as the ability to demonstrate authority but also trust. Your leadership style is collaborative and inclusive, and you have the ability to listen, coach and motivate employees to deliver their best – engaging them in taking pride when meeting their objectives. About the department
Currently, the area consists of 35 highly qualified employees in 3 different teams, but we are growing very fast and expecting to become bigger in the nearest future. We are working in an international environment with many different companies and stakeholders with engagement, trust, and mutual respect. Our performance is driven by the wish to think big, improve and simplify our way of working while ensuring quality compliance, product quality and patient safety. Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career 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. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Vice President, Trine Kantsø at +45-30794362 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 Søborg.
Jobbet er oprettet på vores service den 26.2.2024, 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
- Søborg
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