Validation officer
SIRE
Antwerpen, Belgium
9 dagen geleden

The company

Our client is a professional Pharmaceutical organization, based in Antwerpen Belgium. The client is a leading pharmaceutical in Europe with presence in all European markets.

They have specialists working on its commercial, development and manufacturing operations and manages all aspects of product development, production, marketing, sale and supply.

Role description

You will responsible and support Quality in ensuring that GMP / GDP are pursued. In particular to support product quality by ensuring that protocols are followed up and that data is collected and reviewed and made available to responsible management.

Responsibilities

  • GDP / GMP compliance
  • Validations
  • Perform audits & self-inspections
  • Provide support to the Global Distribution team for ongoing operations and projects deployment
  • Provide training in the field of Quality
  • Identify gaps or non-compliances in the data base and remediate
  • Collect compliance indicating data, review and identify relevant signals
  • Manage monitoring activity
  • Download, review and archive data
  • Requirements

  • A degree in the Life Sciences, with 2 years’ experience in a Quality environment in the pharmaceutical industry
  • Knowledge of GMP and / or GDP
  • Strong communication skills
  • A high level of self-motivation is necessary.
  • Ability to perform audits, internally and externally
  • Dutch and English are required French is a plus
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