Quality enthusiast for QA Lead
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Bagsværd
Are you passionate about quality and want to make a positive impact on patients' lives? We are seeking a skilled QA Lead to join our highly attractive team in Bagsværd.
As a QA Lead, you will play a crucial role in ensuring quality processes in our global network of Contract Manufacturer Organizations (CMOs). In this lead role, you will have the opportunity to make a direct difference every day and participate in various projects working with both internal and external business partners. You will have a high level of complexity and independent decision-making in your daily tasks, and the opportunity to travel to our sites outside Denmark. The Position
In this position, you will have the quality responsibility for technical transfers to CMOs and lead efforts to ensure the CMO Quality Management System (QMS) meets relevant GMP requirements. You will manage quality issues during technical transfers, negotiate and implement quality agreements, approve validation strategies and documents, and set up QA processes for commercial manufacturing. You will also participate in qualification audits at CMOs and ensure follow-up on CAPAs.
Qualifications
You hold an academic degree as Pharmacist, Engineer or similar and preferably have some years of experience from the pharmaceutical industry either from production, QA, or QC where you have gained a solid and up-to-date knowledge of quality and GMP requirements.
We are looking for an open-minded person with an outgoing attitude and natural networking skills, who can perform on different organisational levels.
In addition, we will look for a candidate who
• Has a natural ability to take lead and work as a team player, and proactively contributes to the team’s tasks and activities.
• Has the ability to work in an international set-up with external stakeholders with different interests and agendas.
• Meets own deadlines and knows how to prioritise between different tasks in an everchanging environment.
• Has great communication and collaboration skills and speaks and is fluent in Danish and English. We would enjoy welcoming a straightforward person with a good sense of humour to our department. About the department
GCM QA is responsible for quality assurance and quality support to outsourced production activities worldwide. GCM QA is a dynamic department consisting of 40 competent people divided into 4 teams with focus on either operations or projects. You will be a strong player in the project teams. The department is characterised by a high level of professionalism, flexibility, and cooperation. The primary role of our department is to deliver QA support and set direction for our global CMOs. We focus on good social relations and prioritise to make room for fun at work. We have weekly quizzes, and we strive to have daily workout sessions to ensure on-going well-being in the team.
Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Contact
For further information, please contact Pia Bech Vince on +45 30792171. Deadline
23rd of January 2023
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
Do you know someone?
If it is not the job for you, but perhaps you know someone who might fit and be interested, please share this job. Thank you for your referral.
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 QA Lead, you will play a crucial role in ensuring quality processes in our global network of Contract Manufacturer Organizations (CMOs). In this lead role, you will have the opportunity to make a direct difference every day and participate in various projects working with both internal and external business partners. You will have a high level of complexity and independent decision-making in your daily tasks, and the opportunity to travel to our sites outside Denmark. The Position
In this position, you will have the quality responsibility for technical transfers to CMOs and lead efforts to ensure the CMO Quality Management System (QMS) meets relevant GMP requirements. You will manage quality issues during technical transfers, negotiate and implement quality agreements, approve validation strategies and documents, and set up QA processes for commercial manufacturing. You will also participate in qualification audits at CMOs and ensure follow-up on CAPAs.
Qualifications
You hold an academic degree as Pharmacist, Engineer or similar and preferably have some years of experience from the pharmaceutical industry either from production, QA, or QC where you have gained a solid and up-to-date knowledge of quality and GMP requirements.
We are looking for an open-minded person with an outgoing attitude and natural networking skills, who can perform on different organisational levels.
In addition, we will look for a candidate who
• Has a natural ability to take lead and work as a team player, and proactively contributes to the team’s tasks and activities.
• Has the ability to work in an international set-up with external stakeholders with different interests and agendas.
• Meets own deadlines and knows how to prioritise between different tasks in an everchanging environment.
• Has great communication and collaboration skills and speaks and is fluent in Danish and English. We would enjoy welcoming a straightforward person with a good sense of humour to our department. About the department
GCM QA is responsible for quality assurance and quality support to outsourced production activities worldwide. GCM QA is a dynamic department consisting of 40 competent people divided into 4 teams with focus on either operations or projects. You will be a strong player in the project teams. The department is characterised by a high level of professionalism, flexibility, and cooperation. The primary role of our department is to deliver QA support and set direction for our global CMOs. We focus on good social relations and prioritise to make room for fun at work. We have weekly quizzes, and we strive to have daily workout sessions to ensure on-going well-being in the team.
Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Contact
For further information, please contact Pia Bech Vince on +45 30792171. Deadline
23rd of January 2023
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
Do you know someone?
If it is not the job for you, but perhaps you know someone who might fit and be interested, please share this job. Thank you for your referral.
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 Bagsværd.
Jobbet er oprettet på vores service den 13.10.2022, 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
- Bagsværd
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