Senior Validation Engineer (Denmark, Hillerød)

Jobbeskrivelse
Placering
Hillerød, Denmark

Jobkategori
Manufacturing

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Would you like to apply your skills and expertise to support our production capacity expansion? Does the thought of managing worldwide project excite you? We are looking for a Senior Validation Engineer to join our international team to help us re-design our manufacturing process and automating it without compromising on the quality of our medical devices.

What’s stopping you making a life changing career move - join our Assembly team within Device Manufacturing Development today!

The Position
Our team is constantly growing, which makes this a very exciting time to join Device Manufacturing Development and Novo Nordisk. As Senior Validation Engineer based in Hillerød (DK), 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 who 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 position, we are looking forward to connecting with candidates who:
• Hold at least a bachelor’s degree in engineering (e.g., design, production, process, mechanical) or any other relevant field.
• Have solid experience as Process Engineer within a regulated industry (pharmaceutical, medical devices, food, aerospace, or other), including experience with e.g., validation and risk analysis.
• Are passionate about innovation and have a Lean mindset or related 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 an advantage if you have a previous experience in a medical device or pharmaceutical industry.

As a person, you are well organised, never compromise on quality, and have pragmatic approach in your work. You are willing to act as lead in our lean activities and to challenge the status quo. You will need patience, strong communication skills and good stakeholder management to deal with the local sites and their practices. Being a good team player, you will enjoy collaborating with a wind range of colleagues and stakeholders, 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. Our focus area is the development of new devices, and we are responsible for 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. There is numerous complex and strategic Novo Nordisk projects that we are involved in, which impact the company’s ability to deliver products to the patients, compliance and licence to operate, as well as establishment of the factory of the future on a global level.

Our department, located in Hillerød, includes 50+ highly engaged skilled professionals from 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
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.

Contact
For further information, please contact Manager Airton Miranda at [email protected].

Deadline
14 July 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.