Operator USP/DSP

Eurofins Group; Leiden; Remote; EUR 42,000 - 56,000; Full time

Benefits offered by this job

31 vacation days per year

5 additional vacation days purchase

Sports benefit schemes

Mental health platform access

Flexible start time 07:00–09:00

Training and development opportunities

Job summary

Eurofins Scientific in Leiden seeks an Operator with bioprocessing affinity to contribute to advanced therapeutics production under GMP. You will support scale-up for clinical and commercial readiness in a cleanroom, handling GMP documentation and process investigations.

The role blends hands-on manufacturing with quality documentation, deviation handling, and continuous improvement, within an international Eurofins setting and team environment.

Qualifications

• MLO, HLO or BSc/MSc degree in Biotechnology, Biochemistry, Life Sciences or another relevant scientific field.
• Hands-on exposure to upstream and/or downstream processing through work experience, internships, traineeships or relevant lab/practical education.
• Basic understanding of bioprocessing concepts such as USP, DSP, bioreactors, fermentation, filtration or chromatography.
• Understanding of GMP and the importance of accurate documentation in a regulated production environment.
• Ability to work both practically on the floor and analytically on documentation, investigations and procedural improvements.
• Strong attention to detail and a structured way of working.
• Comfortable working in a dynamic environment with changing priorities and varied responsibilities.
• Able to work independently, while also collaborating effectively within a team.
• Fluent in English, both spoken and written.

Responsibilities

• Executing upstream processing activities, including bioreactor assembly, fermentation and process monitoring.
• Executing downstream processing activities, such as filtration and chromatography.
• Supporting fill line activities where applicable.
• Performing in-process checks and ensuring production steps are executed according to procedures and specifications.
• Reviewing and completing GMP documentation, including batch records, logbooks and data entry.
• Supporting or handling deviations, non-conformances, change controls and CAPAs.
• Updating or improving work instructions and SOPs.
• Contributing to deviation investigation reports and other GMP‑related documentation.
• Participating in process improvements, operational excellence initiatives and cross‑functional projects.
• Supporting 5S and general cleanroom compliance activities.

Skills

Bioprocessing

GMP documentation

Attention to detail

Teamwork

Fluent English

Education

MLO/HLO/BSc/MSc in Biotechnology

Job description

Eurofins Scientificis an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes,France to over 62,000 staff across a network of more than 1000 independent companies in over 62 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

In 2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins PSS Insourcing Solutions®is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client' site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!

Job Description

For our team in Leiden, we are looking for an Operator with experience or clear affinity in bioprocessing within a GMP-regulated environment. In this role, you will contribute to the production of advanced therapeutics and support the scale-up of new products toward clinical and commercial readiness.

This position is broader than a purely hands-on manufacturing role. In addition to executing operational activities in the cleanroom, you will also contribute to GMP documentation, process-related investigations, and continuous improvement initiatives. This makes the role suitable for candidates who combine practical bioprocessing knowledge with the ability to understand and support the quality and documentation side of GMP-manufacturing.

You will work in a cleanroom environment under GMP guidelines, and your responsibilities may include:

• Executing upstream processing activities, including bioreactor assembly, fermentation and process monitoring;
• Executing downstream processing activities, such as filtration and chromatography;
• Supporting fill line activities where applicable;
• Performing in-process checks and ensuring production steps are executed according to procedures and specifications;
• Reviewing and completing GMP documentation, including batch records, logbooks and data entry;
• Supporting or handling deviations, non-conformances, change controls and CAPAs;
• Updating or improving work instructions and SOPs;
• Contributing to deviation investigation reports and other GMP‑related documentation;
• Participating in process improvements, operational excellence initiatives and cross‑functional projects;
• Supporting 5S and general cleanroom compliance activities.

Qualifications

• MLO, HLO or BSc/MSc degree in Biotechnology, Biochemistry, Life Sciences or another relevant scientific field;
• Hands‑on exposure to upstream and/or downstream processing through work experience, internships, traineeships or relevant lab/practical education;
• Basic understanding of bioprocessing concepts such as USP, DSP, bioreactors, fermentation, filtration or chromatography;
• Understanding of GMP and the importance of accurate documentation in a regulated production environment;
• Ability to work both practically on the floor and analytically on documentation, investigations and procedural improvements;
• Strong attention to detail and a structured way of working;
• Comfortable working in a dynamic environment with changing priorities and varied responsibilities;
• Able to work independently, while also collaborating effectively within a team;
• Fluent in English, both spoken and written.

Additional Information

Working at PSS means working in a team where people support each other, take responsibility for their work and stay closely connected to the client environment they work in. You will be part of an international setting, with colleagues who value clear communication, teamwork and a good working atmosphere.

We believe it is important that people can keep developing in your role. That is why we offer specialist training and opportunities to build your knowledge and skills further. We also make time to stay connected as a team, for example through monthly team lunches, team activities and moments where colleagues are recognized for their contribution. We offer:

• A responsible position within the team;
• Room to share your ideas and input;
• Specialist training and opportunities for personal and professional development;
• 31 vacation days per year based on a full-time employment contract, with the option to purchase 5 additional days;
• The option to use gross/net benefit schemes for sports and the purchase of a bicycle;
• Access to an online preventive mental health platform;
• A flexible start time between 07:00 and 09:00, depending on team planning and operational needs;
• A suitable salary and additional benefits.

Working at PSS gives you the personal approach of a medium‑size organization, with the wider network and structure of Eurofins as a parent company. In your work, you regularly interact with other companies and scientists within the Eurofins group, which brings variety to the role.

This also means there may be opportunities to grow, depending on your role, experience and development.