Assistent Scientist USP

For our team in Leiden, we are looking for an Assistent Scientist USP. As an associate scientist USP you have a passion for precision and excellence in laboratory settings.

The lab you’re going to work in supports the Life Cycle Management of commercial products and Secondary Technology Transfers. This lab conducts satellite runs in Leiden for complex investigations, process improvements, and serves as a non-routine sample hub.

Your activities will include:

• Execute experiments and tasks as assigned, following established procedures, and submit data outcomes to management and internal customers.
• Operate and maintain laboratory equipment, ensuring adherence to safety and operational standards.
• Conduct routine testing and analysis to support scientific teams in achieving research goals.
• Manage sample handling, preparation, and storage in compliance with established protocols.
• Document and report data accurately, contributing to technical reports and manuscripts while supporting the laboratory's knowledge base.
• Collaborate with cross-functional teams to optimize laboratory processes and workflows.
• Troubleshoot equipment issues and perform routine maintenance and calibration tasks.
• Actively participate in project meetings and assist team members in achieving research goals.
• Maintain up-to-date lab documentation in accordance with established standards.
• If required for process continuity, perform limited work during weekends and bank holiday.

Qualifications

• Bachelor’s degree in biotechnology, biochemistry, biomedicine, process technology (or equivalent).
• 1-2 years’ relevant work experience in a biotechnology or biopharmaceutical industry environment.
• Practical experience with laboratory techniques and instrumentation for upstream or downstream processing equipment such as bioreactors, AKTA chromatography systems and filtration systems.
• Know-how of laboratory analytical methods such as HPLC, cell count, osmolality, pH and conductivity measurements.
• Knowledge of large molecule drug substance (API) manufacturing process development, root-cause problem solving and lean practices is preferred.
• Familiar with maintaining records of work in the form of laboratory notebooks (paper or electronic).
• Proven ability to follow standard procedures and provide insights for process improvements.
• The ability to report and present findings to peers and project leads.
• Demonstrates a strong commitment to safety, identifies and reports hazards, follows safe work practices.
• Ability to work independently and as part of a team.

Additional information

Working at PSS means working with highly motivated people with a can-do mentality. Our people work in an international environment, within an enthusiastic team and for an organization where there is sufficient room to develop further. Working together is extremely important to us and having fun in what you do is part of that! Our monthly team lunches, team activities and the hand out of awards to our colleagues are an example of this.

We also offer:

• A responsible and challenging position within the team;
• Plenty of room for your own ideas and input;
• Specialist training and a range of opportunities for personal and professional development;
• Flexible working hours;
• Good salary and benefits.

• Plenty of opportunities for growth;
• Varied work where you are in regular contact with other companies and scientists within the Eurofins group;
• A broad customer portfolio ensuring a lot of diversity in your work.