Validation report auditor

Amoria Bond
Geplaatst op
2 tot 6 maanden
Op locatie


Amoria Bond is mediating for a very urgent auditor role at a CRO, focussing on reviewing bio analyses and validation reports. This interim auditor will audit these documents against GxP guidelines. GLP experience is not necessarily required, but desired. GxP experience is obviously a must.

The contract would be for an initial period of 3-6 months with a likely chance for extension. The position is based in the north of the Netherlands, for a minimum of 32 hours per week. A possibility to work 1 or 2 days from home after an initial start-up period can definitely be discussed.

There is already a protocol written, but you do need to know the guidelines and values from GxP/GLP already to ensure quick but perfect solutions. Basically, the job entails correcting other people's work based on GLP guidelines. You need therefore some level of assertiveness.

Interview can be held upcoming Thursday and Friday morning, preferred start-date is asap (literally upcoming Monday if possible, or even sooner). Rates are very good. If you are interested and available, please hit reply and attach your most up to date CV and a quick paragraph on why you are the right candidate.

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 this site.

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

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.

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1 reactie

  • Datum
    19-10-2016 22:59

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