Cleaning Process Engineer

Do you dream about making a true impact when it comes to Cleaning-in-Place (CIP) activities? Would you like to join us from the very beginning of our future journey and make your mark in an organization that will be growing in the coming years? Are you excited about the opportunity to help establish a factory that bridges new and automated technologies with a strong know-how and expertise in biotech manufacturing?

If so, you might be our new Cleaning Process Engineer Apply today for a life-changing career

The Position

As Cleaning Process Engineer, you will participate in project activities for investigating design, constructability, schedule, and cost for a new Recovery facility. In this role, it will be crucial to manage project risks proactively and to develop standards to ensure structure and transparency. You will become part of a dedicated team with a strong focus on implementing known design solutions and developing new ones where relevant.

The key design principle will be to implement the best-in-class design standards from other facilities. Our team participates in a competent user organization, integrating with engineering partners, and collaborating with contractors while supervising their activities.

Main Tasks:

1. Ensure validation of Cleaning-in-Place (CIP).
2. Conduct design reviews.
3. Participate in testing and taking care of all relevant documentation.
4. Perform supplier inspection.

Qualifications

To succeed in this role, you have:

1. Min. bachelor's degree in chemistry, pharmaceutical process engineering, or similar.
2. Solid experience with Good Manufacturing Practice (GMP) and ideally Active Pharmaceutical Ingredient (API) manufacturing.
3. Knowledge and experience related to CIP process and validation of CIP.
4. Fluency in English.

As a person, you are a true team player, who is resilient and a strong motivator to colleagues. Being able to thrive in a multicultural environment that demands independence to make critical decisions, while strongly respecting deadlines is the cornerstone of this team.

While enjoying simplicity, it is essential to build structure in this role. We will welcome a new colleague who is motivated to succeed and has the desire to set a very clear direction.

About the Department

Today, 4,000 employees of Novo Nordisk Kalundborg produce half of the world's insulin and a number of biopharmaceutical products. With more than 50 years of expertise in large-scale biotech manufacturing, we are today the world's largest insulin-producing facility. By joining Novo Nordisk Manufacturing in Kalundborg, we promise you a developing career, where you will be met with trust and responsibility by dedicated colleagues with diverse backgrounds in a successful company with a higher purpose and an inclusive environment. Together, we make a difference every day for more than 30 million people living with diabetes and other chronic diseases.

Interested in a life-changing career? Read more about the opportunities at Novo Nordisk Kalundborg at: Novo Nordisk Kalundborg Careers

Contact

For further information, please contact Senior Project Manager Casper Slots at +45 34485481.

Deadline

31 January 2025.

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.