QA validation specialist
SIRE Life Sciences
Unknown, nl
4 dagen geleden
source : Jobbird

SIRE Life Sciences® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation.

We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies.

By using highly advanced algorithms, we enable our team of Resource & Data Strategists to maintain the most advanced, detailed and complete Life Sciences network in Europe.

This big data enables us to work Reverse Recruitment : we first analyze the market in-depth before we go out to the market.

Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment , making sure we, or better yet, you find the right career!Our client is a professional organisation, based in Flandre Orientale Belgium.

The Company

This company is a global leader in the field of high quality in vitro diagnostics testing. They are a young team where you will have a lot of flexibility.

Role Description

In this role you are gone be the validation specialist within the quality assurance department. Within the organization you will be talking to all the departments.

Everybody will know that they have to come to you for questions and assistance regarding to validation. All the documents, validation protocols and validation rules will be in your hands.

Note : *This is not a validation engineer position*


You will be responsible for all the validation processes that this company has. Making sure the validation strategies and validation protocols are correct and up to date.

Next to that you will be responsible for the following :

  • QA document review
  • Manage and supervise the document flows
  • Judge validation files
  • prepare validation protocols (IQ / OQ / PQ) and approve them
  • Capa's
  • Complaints handling
  • Requirements

  • Bachelor degree or higher
  • 3+ years of experience within pharma, biotech or medical devices industry
  • ISO 13485 (pre)
  • Validation experience (Writing protocols, approving validation documents and validation plans)
  • Wanting to work in a young dynamic team
  • Being able to work with limited supervision
  • Convincing
  • Dutch and English fluent (writing and speaking)
  • Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.

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