Senior Process Validation Engineer

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Hillerød

Are you a seasoned Validation Engineer who is ready for their next challenge? Are you willing to share your knowledge of design manufacturing processes to support our production capacity expansion? Do you have experience of automating processes, without compromising on product quality? Does the challenge of managing worldwide projects excite you? If you would like to join a truly international team then we would encourage you not to waste time and apply today. We would be keen to speak to you about joining our Assembly team within Device Manufacturing Development department. The position As our Senior Process Validation Engineer you will be in charge of development and implementation projects for new assembly production capacities, for our new and marketed products, across multiple geographical locations. You will become a key member of the project and you will:
  • Lead and contribute to validation activities of the project, from basic design and establishing User Requirement Specification (URS) through to process risk assessment and validation (PV) of new production lines.
  • Align local validation practices to ensure the level of standardisation needed to implement multiple lines at different sites is both Lean and conforms with our corporate risk-based validation approach.
  • Be engaged in innovative validation practices, such as remote Factory Acceptance Test (FAT), leveraging validation activities and implementation of ongoing process verification.
    • In return you can look forward to a rich professional experience with strong collaboration with multiple stakeholders from Corporate to local sites, R&D, Production, Suppliers, Quality Assurance (QA) and other specialists in multiple domains. There would also be some travel opportunities. Qualifications For this role, we are looking forward to connecting with candidates who:
  • Hold at least a bachelor’s degree in process engineering, pharmacy or any other relevant field.
  • Have a minimum of 4 years of experience as Process or Validation Engineer within a regulated industry (pharmaceutical, medical devices, food, automotive…).
  • Are fond of innovation and have a Lean mindset or experience.
  • Have a good understanding of science and technical aspects of the manufacturing processes.
  • Are fluent in English (both written and spoken) and experienced with MS Office 365, Teams, e-TIMS and other relevant software solutions.
    • It would be considered as an advantage if you have a previous experience in a 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 and have a pragmatic approach in your work. An innovative thinker, you are willing to act as lead in our lean activities and to challenge the status quo. Patience, strong communicative aptitudes, and stellar stakeholder management skills will help you deal with the local sites and their practices. It is essential that you are a true team-player at heart: you like to collaborate with colleagues and stakeholders in order to achieve common goals. About the department You will join Device Manufacturing Development (DMD) and the assembly department. We are a key function, bridging Device R&D to production. We are involved in the development of new devices, and responsible of the development and implementation of manufacturing capacity worldwide for new and marketed products. We have an end-to-end presence from product development to production implementation and support. We are engaged in numerous complex and strategic projects for Novo Nordisk, impacting the company ability to deliver product to the patients, compliance and licence to operate, as well as establishment of the factory of the future globally. Our department located in Hillerød includes 30+ highly engaged skilled professionals from project managers, specialists, validation, process and science experts. We are collaborating with multiple stakeholders and striving 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, contact Thomas Algot Søllested at +45 3079 7725, or Yannick Segonne at +45 3079 2318. Deadline 28 February 2023. Please note that applications will be reviewed, and interviews will be scheduled on an ongoing basis. 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 22.11.2022, men kan have været deaktiveret og genaktiveret igen.

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