Quality Assurance Private Label Chemicals
8 uur geleden

Job Summary

Our VWR sales channel is a one-stop-shop solution provider for laboratories in a wide range of industries : pharma, chemical, universities, healthcare,.

  • from the smallest -but sometimes critical- item until the most complex equipment, we offer a very wide range of products.
  • On top of that, we provide world-class on-site services so our customers can focus on the areas where they have added value.

    We are currently looking for a Quality Assurance Private Label Chemicals Employee to ensure our products and services meet established standards of quality.


  • Interpret and implement quality assurance standards to assure compliance with GMP, ISO 9001, (ISO 13485) and ISO 17025 and industry regulatory requirements.
  • Draft quality assurance policies, procedures, work instructions and supporting documentation in accordance with the VWR International policy, Legal Environmental & Safety regulation, ISO14001 and OHSAS18001.
  • Interact with company management, internal departments, and other sites to effectively implement and maintain Quality Systems and the accompanying document management systems.
  • Evaluate adequacy of quality assurance standards, review the implementation and efficiency of quality and set up inspection systems.
  • Plan, conduct and monitor testing and inspection of materials and products to ensure finished product quality.

  • Devise sampling procedures and directions for recording and reporting quality data. Collect, compile and analyse statistical quality data to identify areas for improvement in the quality system.
  • Prepare reports to communicate outcomes of quality activities.

  • Investigate customer complaints and non-conformance issues
  • Develop, recommend and monitor corrective and preventive actions
  • Identify training needs and organize training interventions to meet quality standards
  • Perform and document internal audits and other quality assurance activities.
  • Coordinate and support on-site audits conducted by third parties and regulatory agency inspections. Evaluate audit / inspection findings and implement appropriate corrective actions.
  • Implement and monitor risk management activities
  • Ensure up to date batch records and support release of GMP licenced products by the Qualified Person.
  • Ensure the calibration of premises and equipment.
  • Regularly communicate with the production team, QA, QC and Supply Chain responsible to identify opportunities for quality and productivity improvement.

  • You have obtained a higher degree in an applied science, engineering field or chemical background.
  • You are fluent in Dutch and English (and French)
  • You have a good understanding of MS Office software, Excel, Word, PowerPoint, Access and SAP

    For this position, we offer a regular full-time employee contract including a competitive salary with meal vouchers, insurance, bonus system and other benefits.

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