Senior Process Validation Engineer

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Hillerød

Are you a seasoned Validation Engineer prepared to leverage your expertise in designing manufacturing processes to facilitate the expansion of our global production capacity? Have you successfully implemented automated processes while ensuring uncompromised product quality? If you aspire to be part of a truly international team, then we highly encourage you to submit your application today. We look forward of having you join our Assembly team in the Device Manufacturing Development (DMD) department. The position As our Senior Process Validation Engineer, you oversee the development and implementation of projects focused on expanding assembly production capacities for both new and existing products, spanning across various geographical locations. As a key member of the project, your main tasks encompass:
  • Leading and actively participating in project validation activities, from basic design and User Requirement Specification through process risk assessment and validation of new production lines
  • Standardising local validation practices to ensure efficient implementation across multiple lines at different sites, adhering to both Lean principles and our corporate risk-based validation approach
  • Exploring innovative validation practices, including remote Factory Acceptance Tests, leveraging validation activities and implementation of ongoing process verification
    • You can look forward to a rewarding professional experience marked by strong collaboration with diverse stakeholders, spanning Corporate to local sites, R&D, Production, Suppliers, Quality Assurance, and other specialists across various domains. Additionally, there would also be opportunities for travel. Qualifications For this role, we are looking forward to connecting with candidates who:
  • Hold a minimum of a bachelor’s degree in process engineering, pharmacy, or a related field
  • Possess at least 4 years of experience as a Process or Validation Engineer in a regulated industry
  • Demonstrate an affinity for innovation and a Lean mindset
  • Exhibit a good understanding of the scientific and technical aspects of manufacturing processes
  • Display fluency in both written and spoken English and proficiency with MS Office 365, Teams, e-TIMS, and other pertinent software solutions
    • It would be considered an advantage if you have prior experience in the pharmaceutical or medical devices industry. Who are you as a person? Although we try not to place people in boxes, there are some traits that we believe will help you thrive in this role. You are ideally well organised, someone who never compromises on quality while approaching tasks pragmatically. An innovative thinker, you are willing to act as lead in our lean activities and to challenge the status quo. Patience, strong communication abilities, and adept stakeholder management will help you to navigate the local sites and their practices. It’s paramount that you are a true team-player at heart: you excel on collaboration, working seamlessly with colleagues and stakeholders to attain common goals. About the department You will join the assembly department within DMD. We are a key function, serving as a bridge between Device R&D and production. We are involved in the development of new devices, and responsible for the development and implementation of manufacturing capacity for both new and marketed products worldwide. We have an end-to-end presence from product development to production implementation and support, engaged in numerous complex and strategic projects for Novo Nordisk, impacting the company’s ability to deliver product to our patients, ensuring compliance and licence to operate, as well as establishing the factory of the future globally. Our department, located in Hillerød, consists of over 60 highly skilled and engaged professionals, including project managers, specialists, validation, process and science experts. We collaborate with multiple stakeholders and strive for excellence in project execution, science engineering, innovation, and technology. 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 Ariane Giguere-Robert, +45 34 48 32 36. Deadline 28 January 2024. Please note that applications will be reviewed, and interviews will be scheduled on an ongoing basis. Therefore, we encourage you to apply as soon as possible. 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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    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 21.12.2023, men kan have været deaktiveret og genaktiveret igen.

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