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Job position: quality assurance consultant

Location: Belgium

You have experience in quality assurance? You are quality oriented? Then a job as quality assurance consultant in the pharmaceutical industry could be just what you are looking for.

For this position we are looking at all levels of experience, from starter to senior level.

As a quality assurance consultant you work with clients in the pharmaceutical industry to ensure quality on projects or during routine operations. You are or become specialized in the applicable regulatory requirements and the client's quality management system.

Depending on your background and your level of experience in the pharmaceutical industry your responsibilities include:

  • ensure the requirements of the quality management system are applied consistently throughout the client organization
  • manage quality records such as deviations, CAPA's and change controls
  • review and approve GxP documents such as SOP's, WI's, production records, lab results
  • participate to risk assessments and quality investigations
  • follow-up and participate to internal and external audits
  • advise on pharmaceutical regulatory requirements such as GMP, GLP and GDP, taking into account current trends and future vision of the client
  • take decisions which properly balance out quality / budget / planning and help project stakeholders to reach a compromise on critical quality decisions
quality assurance consultants
Quality assurance consultants come in many flavours...
as QA consultant you can become a technical expert, a regulatory expert, project or people manager. Quality assurance offers a career path which is often underestimated in the opportunities it has to offer.

Qualifications

Must have
  • fluent in English, at least conversational level in Dutch
  • a first experience in quality assurance or the pharmaceutical industry
  • strong analytical skills, well organized, studious and precise
  • commercial attitude, able to convince clients by communicating in a clear and enthusiastic way
  • master degree in science or engineering, or equivalent through experience
Nice to have
  • experience working in a GxP environment
  • knowledge of pharmaceutical regulations

Our offer