Nighttime Operator for our Drug Substance Manufacturing team in Upstream

Are you a night owl who thrives when the stars are out? Does it sound attractive driving home through a winter wonderland or catching the sunrise before the world awakens? Do you enjoy having time off when most others are working? Then keep reading. 

We’re seeking a motivated Nighttime Operator (Manufacturing Associate) to join our biopharmaceutical production team in Upstream.
 

The job  
In the position as operator (Manufacturing Associate), you will work on some of the following tasks:  

• Execution and revision of cGMP documents  
• Handling and completion of batch documentation 
• In-process sampling and analytical measurements 
• Execution of validation protocols 
• CiP/SiP of equipment 
• Training new colleagues 
• Reporting deviations 
• Possibility of being a part of different projects such as process optimization, red lining SOPs, 5S and continuous improvements 
   

Schedule & Application 
As an operator (Manufacturing Associate) your work will follow below schedule:  
Week 1: Monday, Tuesday, Friday, Saturday, Sunday 
Week 2: Wednesday and Thursday 
 

Furthermore, you will work on Night 2 (20:05 – 06:18). 
 

Note: First four weeks include comprehensive training from 8:00 – 16:00. 

Qualifications  
We expect from you that:  

• You're the type who double-checks the details and makes sure things don't slip through the cracks. 
• You don't wait to be asked, but step in when something needs to be done 
• You explain things clearly, keep people in the loop, and you are quick to pick up new digital tools. 
• People trust you to do what you say and handle things the right way. 
• You show up with focus and give it your all - even on the routine stuff. 
• You are enthusiastic about working under GMP and you enjoy working with math and IT tools. 
• You have flair for understanding process flows 
• You can read and understand work instructions in English. 
• Experience with working night shifts is a plus. 
   

Preferably, you are experienced in pharmaceutical production or regulated industries OR you are a Life Science Graduate ready to start your career in production. It is a plus if you have experience with cGMP, SOPs, filtration or fermentation processes. 
 

About the team 
You will join a fantastic team of 11 people with diverse backgrounds and an international touch. The team is highly engaged, skilled, and strong in interpersonal collaboration. They are known for their professionalism as well as their sense of humor and strong collegial spirit.
A couple of times a year they also meet outside work for lunch or similar get-togethers.

Application
To be considered for further process, it is a requirement that you submit your application and CV in English.
Deadline is 12th April 2026 but we’re having ongoing interviews, so please do not hesitate to submit your CV/application.

In case of any questions, please send an e-mail to Barbara Lorensen at: barbara.lorensen@fujifilm.com

FUJIFILM Biotechnologies is an industry-leading Biologics Contract Development and Manufacturing Organization (CDMO) with locations in Hillerød, Denmark, Teesside, UK, RTP, North Carolina and College Station, Texas, USA. We use our skills, dedication and ambition to enable impact for the world’s most innovative biotech and biopharma companies reimagining healthcare’s potential. We work across the entire lifecycle of our customers’ products – enabling success throughout. Every cure, vaccine, biologic, and advancement we contribute to starts with our people and our passion. We fuel one another’s passion, help accelerate progress, expand capabilities, strengthen innovation, and improve processes to improve lives. 

Our site in Hillerød, Denmark, brings together expertise, capabilities and technologies to manufacture advanced biologics. The large scale manufacturing facility has a capacity of 120,000 liters to reliably manufacture biologics for late phase and commercial use. We commenced 6 billion DKK projects to double our manufacturing capacity and to add fill finish to the site. 

We offer the chance to be part of a global workplace where passion, drive and commitment are met with opportunities for professional and personal development. Deeply committed to diversity and inclusion, we ensure that everyone no matter their background or gender has an opportunity to develop. We take pride in enriching our communities, caring for our environment, and cultivating a world of opportunity for future generations. 

We aim to foster a collaborative, innovative and rewarding environment, where diverse perspectives and people come together united by a common purpose and shared values. We pursue our fullest potential as individual contributors and team members. We strive to be the employer of choice and we offer a competitive compensation and benefit package. 

As we continue to enhance and expand our capabilities, we are looking for people who share our passion, drive, and energy – what we call Genki – to join our team. 

FUJIFILM Biotechnologies Denmark is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identify or any other protected class. 
 

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.