Process Engineer - Equipment Responsible (Denmark, Hillerød)

Jobbeskrivelse
Placering
Hillerød, Denmark

Jobkategori
Manufacturing

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Are you passionate about designing and validating equipment? Do you want to be a part of Novo Nordisk's most significant expansion project in Hillerød to expand our Active Pharmaceutical Ingredient (API) capacity for Biotech production?

If you can reply positively to these questions, then you might be our new Process Engineer - Equipment Responsible. Apply today for a life-changing career!

The Position
As a Process Engineer - Equipment Responsible, you will join our highly automated Intralogistics team as responsible for the Intralogistics process and equipment. This team is in charge of design and function of the procedures for the Intralogistics equipment. You will join the Intralogistics, Weigh and Dispense department.

This will involve driving the project execution and participate in collaborative design development with suppliers and with oversight to ensure the solution is built according to the design. You will join the team that is at the core of ensuring the best possible design, delivering a solution we can be proud of in 20 years!

We perform reviews of Factory Acceptance Test (FAT), Site Acceptance Test (SAT) protocols and reports, oversee qualification tests, support project team with qualification, deviations etc. You will work in collaboration with a wide network of stakeholders on a local and global level. This will include the Work Package Owner (WPO), operational and engineering responsible, IT/Automation specialist and engineering partners during the project phase. Some travel activities is to be expected.

The main tasks will be to:
• Participate in project execution that will enable a streamlined implementation of the equipment for the Intralogistics.
• Write SOPs, establish the monitoring strategy and training of operators.
• Perform reviews of supplier design documentation.
• Share knowledge with the operational and engineering responsible.
• Align on the technical decisions together with our local project team, central core team stakeholders and the suppliers.

Qualifications
To be considered for this position, you should have:
• A technical degree, bachelor’s or master’s degree in production engineering or similar field.
• Strong experience within a pharmaceutical company with stakeholder management and Good Manufacturing Practice (GMP).
• Knowledge of technical problem solving.
• Experience withing automatic production lines and vision systems, which is considered a plus.
• Fluency in English.

On a personal level, you have a proactive approach when it comes to work tasks. Having great stakeholder management skills and the ability to communicate with colleagues across different job functions, time zones, and cultures is essential to succeed in this role.

About the department
Join us at 25L Active Pharmaceutical Ingredient (API) Capacity Expansion and become a part of one of Novo Nordisk’s most significant expansion projects, embedded in Biotech & Rare Disease (BRD). In BRD, we are building a new API production facility in Hillerød that will employ around 340 colleagues. The highly automated production facility will be equipped with state-of-the-art technology that is flexible to accommodate new processes and products. It will also expand our portfolio of clinical late phase products and increase our capacity to serve more people living with rare disease and serious chronic diseases.

To drive the project and reach the initial phase of production, we need your support. We do not only drive change for our patients – we also drive life-changing careers for our employees by promoting a learning culture with high levels of trust, innovation, and development throughout the organization. Are you ready to join the project team and our journey?

Working at BRD, Novo Nordisk
Biotech & Rare Disease (BRD) is part of Novo Nordisk Product Supply, which is global production network at the front of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.

We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.

Contact
For further information, please contact Manager Anita Pia Thomsen at +45 3075 2020.

Deadline
30 June 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.