Are you a equipment validation engineer and have you worked in a pharmaceutical setting? Are you a self starter and looking for an interesting position in a startup biotech company in Leiden? Read on!
Job Description
Our client has the focus on the development of a novel cell therapy to cure different types of cancers. As they are currently rapidly expanding their business they are looking for a validation specialist (IQ/OQ/PQ) to aid in the validation and qualification of equipment for use in a clinical setting.
You will work on both equipment life cycle activities as well as maintaining the supply chain for laboratory materials that are used on site.
Responsibilities
- Take part in the validation and qualification of new equipment (IQ, OQ. PQ)
- Typical equipment that is used are ELISA, cell counters, and flow cytometry
- Assist in the installation of novel equipment at the client site
- Drafting documentation such as SOPs and Protocols
- Ordering of materials for use in the laboratory
- Oversee incoming goods, registration in LIMS
Requirements
- An MLO/HLO/WO a relevant field e.g. life sciences, biotechnology
- At least 4+ years of experience within validation in a similar (GMP) environment;
- Affinity with operational excellence;
- Affinity with automated systems such as LIMS;
- English is a must, Dutch is considered a plus;
- Valid Dutch work permit is a must;
Benefits
- Contract: 1 year via Oxford, realistic long- term perspective
- Salary: €3100 - €4500 gross monthly based on a full-time position
- Holidays: 25
- Working hours: full-time, 32 hours discussable
- Region: Leiden
- Vacancy number: 19192
