We need someone motivated by regulatory requirements and automated processes to launch important medical devices and combination products. As we expand into a new and exciting Manufacturing Development area within intralogistics, we require a high-performing QA Department to support us. If you're ready to take on this challenge and thrive in a collaborative team environment, apply now! The position
We are seeking an ambitious QA professional to join our team at Device Manufacturing Development (DMD QA), as we are expanding our automated testing facilities and transportation processes for our innovative products within the device and combination products category, impacting both locally and worldwide. In this role, you'll be part of a team setting the compliance direction for operations in transportation, laboratories, equipment, methods, and IT. Among other key responsibilities, you will:
• Set the compliance direction for projects, production-related activities, and maintenance to ensure adherence to relevant regulatory and internal requirements
• Impact a broad range of crucial processes to deliver products to patients, while supporting the new and interesting area of setting requirements for intralogistics that affects Novo Nordisk globally
• Handle documentation, deviations, Change Control, Validation Activities, and possibly new suppliers while supporting departments in Line of Business with regulatory requirements and compliance discussions In this role, you will be able to handle situations independently, apply your subject matter knowledge, identify better practice, create improvements to processes, share knowledge and to let your colleagues learn and shine. Finally, you will find solutions through a solid process and business understanding and give proactive advice to our stakeholders to secure we establish simple compliant solutions within processes. Qualifications
To succeed in this role, you:
• Hold a master’s degree within engineering, Medicine and technology, pharmacy, chemistry, science in transport & logistics, or similar
• Have some years’ experience from laboratory, logistical or QA activities, within the pharmaceutical or medical device industry
• It would be an advantage to have knowledge of device manufacturing, cGMP, validation, Lean and programming
• Preferably have experience with automated processes
• Are fully proficient in English In our recent organizational change, we have started an Intralogistics department, and therefore logistics automation competencies are an advantage, while a high-quality mindset to support this exciting new area is a must. On a personal level, you have outstanding stakeholder management skills and are well-structured in your approach to tasks, thorough and efficient in execution of responsibilities. Your inclusive and respectful mindset will support you in integrating in a diverse team, where we share an informal tone, great work morale and tall ambitions to be the best at what we do. With a healthy sense of humor and a can-do attitude, you will fit right in. We also welcome applicants in the fall of their professional career who would enjoy requiring new competencies. About the department
At DMD QA, we are a team of 31 highly qualified professionals based at our Hillerød site, with diverse backgrounds and interests.
We are responsible for ensuring the quality and compliance of all processes in DMD, including product development and life cycle management, design control, testing, manufacturing development, and manufacturing processes. We take pride in our work and are constantly seeking to improve our competencies and processes through a focus on simplicity and collaboration. By joining our team, you will have the chance to make a real difference in the lives of patients through the development and life cycle management of crucial medical devices. 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
For further information, please contact Associate manager Carlos Gonçalves +45 3079 4194. Deadline
15 March 2024
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.