Quality Compliance Partner
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Søborg
Are you a problem solver with a passion for quality and driving changes? Do you get your energy from working in a global environment and having a large variety of stakeholders? Would you like to be the link between our manufacturing sites and our Headquarter to make sure that high standards for Good Manufacturing Practices (GMP) are implemented, as well as ensuring that we continuously improve and simplify our processes and ways of working?
Then apply today as you might be Quality Compliance Partner we are looking for to join our Local Manufacturing Support department. The position As Quality Compliance Partner you will be responsible for supporting management and your colleagues in maintaining and developing high GMP and quality standards across Local Manufacturing’s global network of sites and Contract Manufacturing Organisations (CMO’s), producing a wide range of products. You will be the point of contact for quality and compliance support, as well as the sparring partner to facilitate alignment and consistency across Local Manufacturing (LM).
Some of your main focus include: Establishing and coordinating Quality network across Local Manufacturing fostering knowledge sharing, alignment and sustainability Driving quality improvements, process improvements and implementation of new requirements/procedures, this also includes planning and execution of workshops as well as monitoring and taking care of the quality heat map Setting direction for audit/inspection planning, in close collaboration with audit/inspection lead and local Quality Coordinators Promoting and nourishing a quality mindset culture and promote knowledge sharing culture across LM. In this position, you can expect a mix of coordination, follow-up, and execution of your own tasks. International travels is another aspect of the role and may be required to visit international sites approximately 3 to 4 weeks per year, possibly more. Qualifications To be considered for this position, we expect you to: Hold at least a Bachelor degree Have preferably a minimum of 5 years of experience obtained within the pharmaceutical or medical device industry Be familiar with production processes, regulatory requirements and quality standards within GMP environment Possess strong stakeholder management and collaboration skills, which allow you to engage and communicate naturally with all types of stakeholders across many different cultures and at all levels Be fluent in English, both written and spoken. It would be considered an advantage if you have experience with coaching of employees and/or management of projects in the context of quality. As a person, you are positive, analytical, action and solution orientated, and you work systematically, logically, and proactively. You are known to think and act with a broad and holistic perspective. You take initiatives on your own, and to ensure commitment from your stakeholders. You have great focus on change management when introducing your ideas and the ability to set direction when it is needed. Your structured approach or project management toolbox helps you follow through and implement your improvement ideas. About the department Local Manufacturing is responsible for establishing and operating local manufacturing production facilities in countries where local presence is required to obtain market access and be allowed to serve the patients. Our production processes are tabletting, aseptic formulation/filling, assembly and pack of diabetes care products for the local markets. We have operating sites and/or projects to establish local manufacturing in Algeria, India, Bangladesh, Saudi Arabia, Japan and other markets. We are approximately 800 colleagues dedicated to drive change for people with serious chronic diseases. Not only are we making a difference for patients – we also strive to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone.
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 Rasmus Sander at +45 3075 5887. Deadline
13 August 2023. Please note that applications will be reviewed and interviews will be scheduled on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few lines 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. 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.
Then apply today as you might be Quality Compliance Partner we are looking for to join our Local Manufacturing Support department. The position As Quality Compliance Partner you will be responsible for supporting management and your colleagues in maintaining and developing high GMP and quality standards across Local Manufacturing’s global network of sites and Contract Manufacturing Organisations (CMO’s), producing a wide range of products. You will be the point of contact for quality and compliance support, as well as the sparring partner to facilitate alignment and consistency across Local Manufacturing (LM).
Some of your main focus include:
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 Rasmus Sander at +45 3075 5887. Deadline
13 August 2023. Please note that applications will be reviewed and interviews will be scheduled on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few lines 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. 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 25.7.2023, 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
- Søborg
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