Home Careers Intern for Validation Engineering

Intern for Validation Engineering

Hillerød, Denmark

Do you have a good understanding of, and interest in equipment and processes including data management and analysis? And are your curiosity and willingness to learn more still intact? Then you may be our candidate for an internship in the Validation Engineering Department, providing an opportunity to dig deep into the basic principles of Large Scale Pharmaceutical Manufacturing.

Job Description

The intern position will be located at the FUJIFILM Diosynth Biotechnologies Site in Hillerød, Denmark. Here, you will be part of the Validation Engineering team, a group vital to keeping a large-scale manufacturing site running on a day to day basis. Specifically, you will be engaging in keeping the 4x process autoclaves in a continuously validated state. This includes planning, generating relevant documentation and executing annual re validations, Performance Qualifications of new autoclave loads and day-to-day interaction with the Responsible Engineers and Manufacturing. Additionally, work might arise relating to the Steam-In-Place (SIP) of process equipment, that will also be in the scope of the responsibilities of the intern position.

All work is done adhering the principles of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP) – both vital aspects of working in the Pharmaceutical Industry.

Additionally, the position will require communication with various stakeholders throughout the execution of validation activities, this being the Engineering Department, Quality Engineering and Manufacturing. This will provide an opportunity to learn the responsibilities of each department, and how they all depend on each other to ensure manufacturing operations runs smoothly.

Qualifications and Education

  • The ideal candidate is well versed in the field of data-analysis and have a good understanding of maths.
  • Good verbal and written English skills
  • Basic understanding of the process of autoclave sterilisation and Steam-in-Place
  • Experienced user in MS office
  • A natural quality-oriented mindset
  • Studying for a Bachelor’s degree or Master’s degree in a relevant field of engineering, pharmaceutical science, pharmacy or chemistry.
  • Have a mind-set of executing while striving for constant improvement
  • Be keen about learning under responsibility

Your Application

If your qualifications are a match to our needs and the job has caught your interest, please upload your CV and your application as soon as possible and latest by November 30th.

Start date: 1st of February if possible

Apply Here

FUJIFILM Diosynth Biotechnologies is a world leading cGMP Contract Development and Manufacturing Organisation (CDMO) with over 25 years’ experience. As a world leading CDMO we combine technical leadership in cell culture, microbial fermentation and gene therapies with state of the art GMP manufacturing, from our network of four global locations in the USA, UK and DK. We currently employ over 2,000 dedicated staff who have a reputation for excellent customer service, flexibility and responsiveness. 

As part of FUJIFILM Diosynth Biotechnologies you will be an active contributor in the advancement of tomorrow’s medicine. We take pride in enriching our communities, caring for our environment and cultivating a world of opportunity for future generations. We invest in you and what you care about, getting the right work-life balance for your health, your family and your professional growth. 

FUJIFILM Diosynth Biotechnologies offers a healthy work environment that promotes individual responsibility, allowing you to grow and progress. We support our employees with programs that motivate and educate, promoting a healthy work-life balance that ultimately increases personal well-being and employee satisfaction.