Quality Compliance Specialist - Biotech Company - 6 Months

For a project of 6 months with start-date March, an international pharmaceutical biotech company in the North of the Netherlands is now looking to temporary expand their quality department with an experience Quality Compliance Manager Systems.

The profile and inherent responsibilities would look like this:

*Good knowledge of Quality systems in general
*Working with validations, clean room, monitoring, KPIs, audits, supplier qualifications, regulatory, via GMP guidelines
*Expertise on how quality systems are put together and how to do validations in equipment, utilities, supplier audits etc.
*Being able to take initiative
*If possible, leading the systems team consisting of three other people

A background in biotech and speaking Dutch are a large advantage and rates are depending on expertise, but more than fair. Screenings by Amoria Bond will be held early next week, client interviews are later that week.

Candidates whom are interested or want to learn more about the role or position, can send an e-mail with their CV (in word-format) to Christiaan de Wit at (see below)

Key search terms: Quality, compliance, systems, quality systems, QS, manager, GMP, good manufacturing practice, farma, pharmaceutical, biologics, biotech, biotechnology, biology, QA, Freelance, Interim, zzp, contract, project, temporary,

Disclaimer: Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age and experience, and we confirm that we are happy to accept applications from persons of any age and experience for this role.