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Validation Engineer

  1. Antwerp
  1. Contract
Competitive
26044//AS
  1. Commisions, Qualification and Validation
Date Posted13 Jan 2021
Our global bio-pharmaceutical client is seeking the expertise of a Validation Engineer to support their state-of-the-art facility in Belgium. This role requires English and Dutch languages. It will be home based where possible but involve travel to site when required.

The purpose of this role is to:
  • Perform activities necessary for qualifying and validating devices, systems, software and processes
  • Investigate and solve validation-related problems and write documentation for new and / or existing validation activities
  • Work to predefined procedures and system standards in order to guarantee compliance with company standards and cGMP regulations

Responsibilities:
  • Perform validation activities; and proactively providing advice, service and technical expertise
  • Monitoring validation processes; adjust and / or escalate where necessary
  • Proactively following up on developments within your own field as well as building and sharing knowledge within this domain
  • Initiating and conducting specific research into existing and innovative processes and technologies, as well as developing and implementing new (sub) processes and technologies
  • Initiate consultation with experts across disciplines
  • Prepare, maintain, check / review, approve and implement validation and other quality-related documentation
 
Background:
  • Master's degree in life sciences or Bachelor with more related experience
  • Experience in a validation focused role
  • Good knowledge of cGMP
  • Dutch and English language

If you would like to learn more about this role, please apply today!

The candidate must have the rights to work in the location stated in the job advert.

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Description

Our global bio-pharmaceutical client is seeking the expertise of a CSV Engineer - Computer Systems Validation - to support their state-of-the-art facility in Belgium. This role requires English and

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