GMP Bioprocess Operator – USP/DSP, Cleanroom

Eurofins; Leiden; Remote; EUR 42,000 - 65,000; Full time

Benefits offered by this job

Specialist training

Personal development opportunities

Online preventive mental health平台

Team lunches

Job summary

Eurofins Scientific in Leiden is seeking an Operator with affinity in bioprocessing within a GMP-regulated setting to contribute to the production of advanced therapeutics and support the scale-up of new products toward clinical and commercial readiness.

You will work in a cleanroom environment, perform upstream and downstream processing activities, and contribute to GMP documentation, investigations and continuous improvement, collaborating with cross-functional teams.

Qualifications

• MLO, HLO or BSc/MSc 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

Upstream/downstream

Teamwork

Attention to detail

Education

MLO/HLO degree

Biotechnology degree

Life sciences degree

Job description

Eurofins Scientific in Leiden is seeking an Operator with affinity in bioprocessing within a GMP-regulated setting to contribute to the production of advanced therapeutics and support the scale-up of new products toward clinical and commercial readiness.

You will work in a cleanroom environment, perform upstream and downstream processing activities, and contribute to GMP documentation, investigations and continuous improvement, collaborating with cross-functional teams.