Location: Oss, The Netherlands
Work model: On-site
Employment type: Full-time
About the role
For a biopharmaceutical laboratory environment in Oss, we are looking for an Associate Scientist DSP.
In this role, you will work within a small-scale downstream processing team, focusing on the purification and analysis of samples from production and small-scale studies. You will perform hands-on laboratory work in a regulated environment where accuracy, documentation and compliance with quality guidelines are essential.
This is a full-time, on-site position in Oss.
Key responsibilities
- Perform immunopurification on samples from production and small-scale studies using ÄKTA systems.
- Perform capillary zone electrophoresis on immunopurified biopharmaceutical samples.
- Carry out additional DSP-related activities, including purification and analytical work.
- Record activities, results and deviations in laboratory notebooks according to applicable documentation requirements.
- Share progress, results and points of attention during team meetings.
- Participate in daily alignment meetings regarding planning, priorities and ongoing laboratory activities.
- Maintain laboratory equipment, including quality checks and calibrations.
- Perform basic IT-related laboratory tasks, such as software installations, user management and support with system access.
- Support documentation activities, including writing or updating protocols, work instructions and reports.
- Identify improvement opportunities in laboratory processes, documentation, equipment use, planning or collaboration with other teams.
Requirements
You work accurately, take ownership of your tasks and understand the importance of traceable and reliable laboratory documentation. You are comfortable working in a structured laboratory environment and can plan your daily activities based on priorities, sample availability and deadlines.
You do not need to be a senior specialist, but you should be proactive in identifying practical improvements and willing to contribute to a more reliable, efficient and transferable way of working.
Your background
- Completed MBO or HBO education in a relevant field, such as Life Sciences, Biochemistry, Chemistry or a related discipline.
- Hands-on experience with downstream processing in a biological or biopharmaceutical environment.
- Knowledge of quality standards such as GLP and/or GMP, preferably gained in a laboratory or production environment.
- Experience with ÄKTA systems is a strong plus.
- Experience with Empower and/or Unicorn software is a plus.
- Good command of Dutch and English, both written and spoken.
- Strong attention to detail and the ability to document work clearly and accurately.
- Ability to work according to laboratory priorities, sample availability and deadlines.
- Practical mindset and willingness to contribute to process improvements.
What you can expect
You will work in an international and quality-driven laboratory environment with motivated colleagues and a strong focus on collaboration, development and continuous improvement.
The position offers varied work, room for your own input and opportunities for personal and professional growth. You can expect specialist training, development opportunities, good employment conditions and a working environment where teamwork and quality are central.