Analyse pharmaceutical raw materials and finished products in a Quality Control laboratory in Leiden. Manage lab equipment and document work. Full-time, 40 hours per week, on a 12-month temporary contract.
The role
As a Laboratory Analyst in Quality Control in Leiden, South Holland, you will analyse pharmaceutical raw materials and finished products in line with approved procedures. You will manage and maintain laboratory equipment and carry out related tasks, including sample management, review activities and administration.
Responsibilities
- Analyse raw materials and finished products according to approved procedures.
- Manage equipment, standards and chemicals, and maintain the associated logbooks.
- Report work using laboratory notebooks and LIMS.
Your profile
- Completed laboratory education at HBO level, or MBO education combined with work experience.
- Experience in a regulated GMP environment, such as pharmaceuticals or food, is preferred.
- Excellent spoken and written Dutch and English.
- A technical mindset.
- Commitment to the mission and product quality; an entrepreneurial, collaborative and solution-focused approach.
- Flexible and willing to learn, reliable and energetic, with a respectful, honest and transparent manner.
Hours and contract
- Full-time: 40 hours per week.
- Temporary contract for 12 months.
- No specific shift pattern is provided.