- Location:
- Hillerød – Frederiksborg, Zealand, Denmark
- Salary:
- Competitive
- Type:
- Permanent
- Main Industry:
- Search Engineering Jobs
- Other Industries & Skills:
- Manufacturing
- Job ID:
- 131247389
- Posted On:
- 19 October 2024
Are you looking for an exciting international job as Quality Responsible for suppliers worldwide? Do you enjoy collaborating, coaching and challenging external partners and being part of a supporting and dynamic team?
Then we might have the right opportunity for you in Global Contract Manufacturing Devices QA (GCM Devices QA) in Novo Nordisk, read more and apply now!
The position
In this role, you will independently – and with the support of your colleagues and via close dialogue with process experts, supply managers, Manufacturing Science & Technology and R&D – have the responsibility for the quality output of our suppliers, who are working within the fields of injection moulding, advanced assembly processes, electronic production and metal processing.
Your main responsibility is to oversee the quality of the products our suppliers deliver. This includes creating and maintaining quality contracts, handling of deviations, change control and facilitating continuous improvement without compromising patient safety.
Around 20 travel days a year can be expected, to support building relations and expanding your knowledge in a complex and challenging business environment. Quality mindset, simplicity and Winning culture are integrated concepts in our work. You will find that you have rich opportunities to create great results and develop yourself, both on a professional and on a personal level, and you will be trusted to execute your great ideas.
We offer an internationally exciting job with lots of challenges. We implement individual development plans which support your growth and assist you in achieving your professional ambitions. We ensure that there is a good work-life balance, share an informal tone, and enjoy learning from each other, striving to deepen our understanding of an increasingly complex area.
Qualifications
To be successful in the role we envision you as someone who works independently and is not afraid of taking the initiative, while always seeking to develop yourself.
Ideally, you:
-hold a M.Sc. within relevant engineering area
-have worked within quality assurance with external suppliers
-have preferably worked for the medical devices industry
-are fluent in English, both written and spoken
It will be seen as an advantage if you have experience with validation, ISO13485, GMP, Lean manufacturing and systematic problem solving.
On a personal level, you are strong in forming and maintaining relationships with stakeholders across and beyond the organisation, also thanks to your strong communication skills. You are great at engaging and managing stakeholders, and your direction-setting initiative is rivalled only by your ability to follow through and your keen appreciation of quality. You enjoy sharing your knowledge, providing support for your colleagues when they need this.
If you have a different educational background or a are newly graduate, but shares our passion for Quality, GMP and problem solving don’t hesitate for the position or call to learn more about the position.
About the department
In GCM Devices QA we are responsible for the quality of components for Novo Nordisk medical devices. Our suppliers are located in Europe, China, & Brazil.
We are part of the Novo Nordisk Quality organisation where we enforce compliance on behalf of authorities, support the business and at the same time strive towards making daily work for ourselves and our stakeholders less complex.
The department consists of 12 highly qualified QA Engineers who have the responsibility for the quality of metal, electronic and plastic components produced by Novo Nordisk suppliers. We work in lovely surroundings in GCM Devices buildings in Hillerød about 30 km north of Copenhagen.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
If you want to know more about the position, Senior Manager René Bohnstedt Schnack +45 30 75 92 70.
Deadline
3 November 2024
Please note that applications will be reviewed on an ongoing basis, and interviews will be scheduled as soon as relevant candidates are identified, so we encourage you sooner rather than later.
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.
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