Associate Manager for QA operations team

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Hillerød

Are you ready to lead and motivate a team of highly skilled employees, who together with the Internal QA Operations team are responsible for Quality Assurance of the internal operation in Device Manufacturing & Sourcing (DMS)? Do you have a patient-centered approach to your decision-making, a high-quality mindset and great collaboration skills? Do you want to be part of a leadership team that focuses on bringing out the best in each other? Then you might just be the leader we are looking for in Device Manufacturing and Sourcing Quality Assurance (DMS QA) – and we look forward to making you feel welcome here. The position As Associate Manager for Internal QA Operations support, you will lead, coach, and develop a team of 10 highly dedicated and competent employees. Your area of Quality Assurance responsibility covers all the operations support processes e.g., Supply chain, Warehouse, IT/Data, Training, and Audit. The team is also responsible for the release of all components for Novo Nordisk pen systems from our global network of external suppliers. In this position, you will be collaborating closely with key stakeholders across the entire device value chain to ensure that we deliver the highest quality to our patients promptly. Moreover, you will drive the optimization of our quality processes and systems in a GXP compliant and strategic business value-adding way. Participation in audits and inspections is part of the role. As part of the management group in DMS QA, you will be responsible for aligning common goals and strategies and implementing them in your area. You will need to have a high degree of readiness for change and be ready to adapt, as new priorities can arise from day to day, and collaboration across the whole department is necessary to succeed. You will play an active role in setting the direction for the area and contribute to cross-team initiatives and projects. You will report to the Director of Device Manufacturing and Sourcing QA. Qualifications To succeed in this position, you: - Hold a Master’s degree in Engineering, Pharmaceutical sciences, or a related discipline. - Have a strong quality mindset and preferably experience from working within Quality Assurance or the medical device area. - Have knowledge of Novo Nordisk’s organization and product portfolio, as well as quality and/or production processes from previous jobs is an advantage. - Are fluent in English and Danish. As a person, you are proactive, curious, ambitious, have a great interest in developing yourself, and have a good sense of humor. You thrive in a dynamic environment with many simultaneous tasks and upcoming priorities and always meet strict deadlines and business targets. You have strong interpersonal skills and a proven ability to network, build trust in your relationships, and get commitment from internal and external stakeholders. About the department DMS QA is located in beautiful surroundings in Hillerød, 30 km north of Copenhagen. The department consists of 44 dedicated Quality engineers, QA technicians and QA professionals and are still growing. The area currently contains two teams but will be organized in four by March 1st. The department is responsible for the quality assurance of the in-house production as well as the global supply chain of high quality components and preassembled parts for all Novo Nordisk prefilled and durable devices. Our external suppliers are in Europe, China, USA and Brazil. The main purpose of DMS QA is to safeguard patient safety, product quality and compliance. 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. Being a part of Novo Nordisk’s Device Manufacturing and Sourcing QA organization (DMS QA) means working with a global focus at one of the world’s largest and most successful pharmaceutical companies. Our DMS QA organization is a vital part of Novo Nordisk’s delivery to our patients, and we always welcome talented people who value a collaborative environment and would like to grow with us. Contact For further information, please contact Hanne Lindvig Ziegler at +45 3079 7812. Deadline 2. January 2024. Please note that applications will be reviewed continuously, and interviews will be scheduled as soon as a suitable candidate is identified. 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 14.12.2023, men kan have været deaktiveret og genaktiveret igen.

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