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QA Auditor I - Netherlands  

Charles River (company)


Posted on : 13 August 2017

Project Description

The organization employs ~ 10,000 staff worldwide. Our company here in the Netherlands is a well-known, internationally operating contract research organization. The company specializes in areas such as environmental and safety research for new and existing drugs, chemical substances and products. Quality-thinking is the essence of our company. Our clients are international pharmaceutical, chemical and agro-chemical companies.To accomplish this challenging and varied work we are looking for a:

Job profile:
  • Performs audits of protocols, in-life critical phases; raw data and final reports to assure compliance with Good Laboratory Practice Regulations (GLP) and Standard Operating Procedures (SOP);
  • Delivers advise to our company  staff (including management and study directors) on issues relating to GLP compliance;
  • Performs process and facility audits and reviews corresponding regulatory documentation to ensure compliance;
  • Assists in vendor and subcontractor audits;
  • Assists with sponsor and regulatory agency site audits;
  • Assists with harmonizing and improving quality processes;
  • Provides training for our company  staff to leverage their knowledge and understanding of GLP compliance and other relevant quality systems.

Your profile:
  • A bachelor degree in a scientific discipline;
  • Experience with GLP or a comparable quality system;
  • Strong knowledge of Dutch and English;
  • Good communication and advisory skills;
  • Work as a team member;
  • Accurate and quality minded.

We offer:
  • A challenging and independent position in a dynamic environment;
  • The possibility to develop further in a global team;
  • Good primary and secondary working conditions;
  • An open company culture with an informal atmosphere.