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The Senior Technician in Process Development plays a critical hands-on role in supporting the design, execution, and optimization of laboratory-scale processes within R&D. This individual is responsible for conducting experiments, maintaining laboratory equipment, ensuring data integrity, and contributing to the reliability and efficiency of process development activities. With strong technical expertise and a commitment to quality, the Senior Technician ensures that all laboratory operations comply with internal standards and regulatory expectations, while actively supporting innovation and continuous improvement. This role is essential to the success of process development projects and serves as a key contributor to the scientific rigor and operational excellence of the R&D function.
Job Responsibility:
Execute laboratory experiments related to process development and optimization
Support the creation, refinement, and validation of laboratory-scale models
Follow standardized protocols and SOPs
Accurately record experimental data
Assist in the development and troubleshooting of laboratory-scale models
Contribute to process improvements
Collaborate with process development and analytical teams
Perform routine and non-routine analytical testing
Conduct equipment startup, shutdown, and basic maintenance tasks
Support the calibration, qualification, and preventive maintenance of laboratory equipment
Ensure proper storage, handling, and traceability of reagents, consumables, and materials
Participate in 5S, housekeeping, and safety programs
Review experimental data for accuracy, consistency, and completeness
Interpret results from analysis reports
Escalate deviations or unexpected findings
Maintain strict adherence to data integrity principles
Work closely with R&D scientists, analytical teams, and manufacturing personnel
Act as a liaison between R&D and production
Contribute to team discussions and improvement initiatives
Support the training of junior staff and interns
Promote best practices in laboratory operations, documentation, and quality compliance
Share knowledge and experiences
Requirements:
Bachelor’s degree in Biotechnology, Biochemistry, Pharmaceutical Sciences, or a related scientific field
Minimum 3–4 years of hands-on experience in process development within a pharmaceutical, biotechnology, or life sciences environment
Proficiency in key laboratory techniques, including: Ultrafiltration/Diafiltration (UF/DF), Chromatography (e.g., AKTA, NGC systems), Filtration and membrane technologies
Experience with laboratory equipment maintenance, calibration, and troubleshooting
Familiarity with GxP principles and quality systems (e.g., EU GMP, ICH Q7)
Proficient in MS Office and relevant data management tools
Strong attention to detail and commitment to accuracy and quality
Organized and capable of managing multiple tasks efficiently in a fast-paced environment
Team-oriented with a proactive, solution-focused mindset
Excellent verbal and written communication skills in English, with fluency in French and/or Dutch preferred
Willingness to learn, adapt, and share knowledge across teams
Understanding of GxP requirements within the scope of responsibilities
experience in writing or reviewing GxP documentation (e.g., deviations, change controls, sample requests)
Nice to have:
Fluency in French and/or Dutch preferred
What we offer:
Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees
Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutions sectors on impactful missions
International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe