Laboratory Technician / Analyst – QC Chemistry

A broad analytical role in QC Chemistry

We are looking for a laboratory technician / analyst who enjoys variety. You will work across several analytical methods, products and practical laboratory tasks rather than specialize in only one technique.

You do not need experience with every method we use. What matters is that you take responsibility for your work, learn new methods, ask for help when needed and contribute wherever the laboratory has the greatest need.

About FUJIFILM Biotechnologies and Quality Control

FUJIFILM Biotechnologies is a contract development and manufacturing organization (CDMO). At our Hillerød site, we support customers from early development through commercial GMP production.

Quality Control (QC) in Hillerød includes around 300 colleagues in testing and support teams. We work across teams to solve problems, meet shared priorities and improve how the laboratory operates. The organization is relatively flat, so ideas and decisions stay close to the work.

About the QC Chemistry Department

QC Chemistry consists of 40+ colleagues across three teams (analysts, scientists, students and leaders). We support global release of commercial DS/DP using compendial and platform methods (e.g., CESDS, IcIEF, SDS-PAGE, HPLC/UPLC, appearance, pH, osmolality, SoloVPE/UV). We also handle TOC changeover/cleaning validation and testing of utility gases and water. With site expansion and a new Fill & Finish facility, method transfers, validations and qualifications are growing. We qualify controls and reference standards and manage deviations, CAPAs, invalid assays, OOS and Change Controls to keep products moving safely to patients.

The role - what you’ll do

What the working day is like: Around 50% of the role is routine testing. Assignments and methods may change from day to day, and priorities can shift at short notice when samples, instruments or production needs require it. You will belong to one QC Chemistry team and plan your own day in close coordination with your colleagues. Qualification in a new method can take from a few days to several weeks, depending on the method and your previous experience.

• Perform routine and non-routine testing across several analytical methods.
• Move between product testing, stability samples, method activities and practical laboratory tasks.
• Learn additional methods over time instead of working permanently within one analytical area.
• Investigate unexpected results and instrument or method issues together with colleagues.
• Help keep the laboratory running through documentation, reagent qualification, instrument follow-up and other shared tasks.
• Support method transfers, qualifications and validations when relevant.

About you

Being proactive in this role means planning and following up on your own tasks, speaking up early when a result, instrument or deadline is at risk, and involving the right colleagues to find a solution. When priorities change, you adjust your plan and coordinate with the team. You are willing to learn new methods, take on different types of analysis and help with shared laboratory tasks when needed.

• Education: Trained Laboratory Technician or another relevant laboratory-based qualification.
• Experience: At least 5 years of hands-on laboratory experience is required. Experience from pharmaceutical production, quality control or another regulated environment is an advantage, but we will provide training in our specific methods and systems.
• Methods: Hands-on experience with one or more analytical techniques, such as chromatography, electrophoresis, spectroscopy or general physicochemical testing. Experience with HPLC/UPLC, CE-SDS, IcIEF, CESDS, SDS-PAGE, pH, osmolality or SoloVPE/UV is useful, but you are not expected to know all our methods when you join.
• Skills: You work carefully and methodically, document your work clearly and can interpret results and basic statistical data. You are comfortable using electronic laboratory systems such as LIMS or Empower, or able to learn them. You give concise updates, raise concerns early and suggest practical next steps.
• Language: You can read, write and communicate clearly in English in a regulated laboratory setting. Danish is an advantage, but not a requirement.

What we offer

A role in a growing company with room for responsibility, learning and development. You will join a helpful team with strong technical expertise and a good sense of humor. Benefits include competitive pay and bonus, health insurance, health checks, on-site fitness, café and canteen, Friday brunch, monthly cake and our bell-ringing tradition for milestones.

As a general rule, we work on site because the role is laboratory-based. You plan your own day, and when your tasks consist of SOP reading or other computer-based work that can be done remotely, working from home can be agreed with your manager.

Application

Send your CV and a short cover letter as soon as possible and no later than 20 November 2026.

Questions - please contact:

Associate Manager Maja Rydahl at maja.rydahl@fujifilm.com

Working at FUJIFILM Biotechnologies

We offer a competitive compensation package in a site/company growing rapidly, with many opportunities for individual growth. We also offer access to fitness and an attractive canteen.

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 Manufacturing site in Hillerød, Denmark, brings together a complete range of expertise, capabilities, and technologies to manufacture advanced biologics. 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.

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 offer a competitive compensation and benefit package.

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 identity, 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.