Associate Manager

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Hillerød

Do you want to be part of a fantastic QA management team that values team spirit, empowerment, and good collaboration with our stakeholder? Are you passionate about motivating and supervising a team and helping them perform at their best? Can you picture yourself working in a great team with passion for Quality Assurance and thriving by launching important medical devices and combination products to patients in need? If yes, apply now for a life changing career as an Associate Manager for Device Manufacturing Development QA. The position We are looking for an Associate Manager for our QA team of approximately 14 highly skilled dedicated employees, and you will play a key role in managing, developing and shaping your team and improve how we work with quality assurance. Your main task will be to coordinate and develop your team, coach and train the employees to ensure the right composition of skills to address current and future needs.The team is responsible for setting the compliance direction and advice our colleagues on compliant solutions across the organisation within product development and product maintenance of medical devices and combination products including related laboratory activities. Your key to success lies within your ability to perform as an inspiring, coaching and motivating leader and, at the same time practise good stakeholder management in a complex and dynamic organisation. In addition, you will be part of the experienced management group and will work closely with your management colleagues on day-to-day operations and people management-related matters. Qualifications To succeed in this position, you have: • Master’s degree in Engineering, Chemistry, Pharmacy or similar combined with a solid experience from the pharmaceutical or medical device industry • Ability to set directions, ensure compliance in close collaboration with your team and stakeholders • Experience as people manager • Good and clear communication skills in English • The ability to set direction and to ensure compliance, in close collaboration with your team and stakeholders. Preferably you worked before with medical devices and combination product, as well as know about Design Control, experienced with interpretation of relevant regulatory requirements and standards.As a person, you have strong quality mindset and high level of dedication with an interest in leading high skilled people, together you thrive in a constantly changing and challenging environment. Lastly, you are well organized and create strong results by engaging your employees in taking pride in delivering on their objectives. As a leader, you see and match your employees' needs and ambitions. About the department Our department consists of approx. 30 highly qualified employees. We take pride in our work, are located at Site Hilleroed and are responsible for assuring quality and compliance of all processes in Device Manufacturing Development (DMD). This includes product maintenance, design control, testing, manufacturing development and manufacturing processes. Both internally in Device Manufacturing Development (DMD), and in the rest of Novo Nordisk we have many key stakeholders due to the nature of the processes. We are constantly improving our competencies and our way of working by focusing on simplicity and good collaboration to be able to deliver the best possible support to the business. 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 50,000 employees. Together, we go further. Together, we’re life changing. Contact For further information please contact Director Jacob Stenmann Valsborg at +45 3075 4798 Deadine March, 15 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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Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Hillerød.

Jobbet er oprettet på vores service den 28.2.2023, men kan have været deaktiveret og genaktiveret igen.

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