JOB DESCRIPTION
Contract Type
Candidate (Freelancer)
Company Type
Biotech
Company Size
Startup < 100
Requested Expertise
Pre-Clinical Research / Quality / Clinical study / Clinical development
Profile Required
– Experience with pre clinical CRO audit for Toxicology studies
– Compliance with GLP, GCP, ISO 10993
Project Description
The company is looking for an auditor to conduct an audit of a Pre-Clinical CRO site (Contract Research Organization) in accordance with Good Clinical AND laboratory Practices. The audit concerns toxicology activities (in vitro and in vivo tox studies).
Main details regarding the audit:
– Scope of the audit: In vitro and in vivo toxicology activities (6 months on Rats)
– Applicable standards: ISO 10993, GLP, GCP
– Site address: Chasse-sur-Rhône
– To include: audit preparation with the company + 1 audit day on site + edition of audit report in english , review of CAPA plan
Therapeutic Area
Diabetes,Surgery
Language
English,French
Hard Skills
Fluency in French,Fluency in English
Soft Skills
Seniority Level
Experience 5 – 10 years,Experience > 10 years
Starting Date
2025-05-01
Project Duration
Around 4-6 days
FTE / nb of days per week
1
Project Location
France , France
Remote Flexibility
Yes
Travel Expected
Yes
Approximative Budget
Any other information of interest
or recommend someone & get 1000€ from pharmatch.co !
contact@pharmatch.co