Are you looking for an exciting international job as quality responsible for suppliers worldwide? Are you good at collaborating! Coaching and challenging our external suppliers on a daily basis? Be a part of a Global expansion of suppliers? If you can see yourself in a department with great colleagues and world class ambitions, then we may have just the right job for you in the quality assurance department of Device Manufacturing & Sourcing. DMS external manufacturing QA.
In DMS External Manufacturing QA we seek an enterprising and engaged engineer who will be responsible for the quality assurance of certain components for Novo Nordisk medical devices. Our suppliers are located in Scandinavia, Europe, China, USA & 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.
You will independently, with the support of your colleagues and via close dialogue with process experts, supply managers, Device Manufacturing Development and R&D, have the responsibility for the quality output of our suppliers. Your main responsibility is to oversee the quality level of products our suppliers provide. This includes creating and maintaining quality contracts, handling of deviations, change control, and facilitating continuous improvement without compromising patient safety. Our suppliers are working within the fields of injection moulding, advanced assembly processes, electronic production and metal processing.
Around 20 travel days a year can be expected, 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. We share an informal tone, and we enjoy learning from each other, striving to deepen our understanding of an increasingly complex area.
As the ideal candidate you have previous experience within quality assurance, have worked with suppliers in a global environment and with advanced assembly or moulding processes.
• You have a Master´s degree within the fields of mechanics/electronics/manufacturing or have a similar engineering degree.
• Knowledge of ISO13485, cGMP, validation, Lean and programming is an advantage. You are fluent in English, both written and spoken.
• On a personal level, you are ambitious and have a great interest in developing yourself.
• You make a difference and through your commitment and perseverance, you complete your tasks in close cooperation with your colleagues.
• You are collaborative and enjoy sharing knowledge and experiences with stakeholders. You're independent and not afraid to take the initiative.
We also welcome applicants from other branches, as long as you share our passion for quality, GMP and problem-solving and are keen to acquire professional competencies to become what we describe as an “ideal candidate”.
Also, if you are in the fall of your professional career and would enjoy requiring new competencies you are most welcomed to apply.
Let’s talk, even if you are looking for a position with reduced hours.
About the department
The department consists of 15 highly qualified QA engineers who have responsibility for the quality of electronics, springs and plastic components produced by Novo Nordisk suppliers. We work in lovely surroundings in Novo Nordisk Device Manufacturing and Sourcing's buildings in Hillerød about 30 km north of Copenhagen.
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