QA Specialist

  • The Randstad, The Netherlands
  • 6000.00 - 7000.00
  • 32-40 uren
  • HBO


Our client is a consultancy in the food and pharmaceutical industry.


Our client is a consultancy in the food and pharmaceutical industry. They participate in very attractive projects for experienced engineers in the pharmaceutical industry. They offer challenging, varied projects with ample opportunities for personal contributions and development.

functie Vereisten

  • Technically skilled – general understanding of analytical method validation is required
  • Independent and organized accurate worker, with eye for detail
  • Effective stakeholder manager, able to influence. The ‘go-to’ person on difficult content issues
  • Is pro-active in the identification of issues, has problem-solving capabilities, and timely implements solutions
  • Communicates effectively with professional staff and leadership across departments
  • Is able to think and challenge beyond own expertise area, conceptual (end to end) thinker
  • Education: MSc in a relevant discipline, like Pharmacy or Bio-Pharmaceutical Sciences
  • Languages: English
  • Experience: 5+ years of analytical experience in an pharmaceutical setting, preferably in Quality Assurance / Quality Control / Analytical Development

Wat krijg je?

  • Pension entitlement as from day one
  • Collective WGA / WIA insurance
  • NBBU / ABU collective labor agreement
  • 25 holidays days
  • 8,33% holiday allowance
  • 100% payment in case of illness after one waiting day
  • Travel allowance


Currently our client is searching for a QA Specialist. In this role you will work in a multidisciplinary and dynamic team to oversee the technical and analytical development, mainly QA oversight on analytical development teams, review of method transfer documentation and issue handling for analytical method transfers to external manufacturing sites and laboratories worldwide.

Key responsibilities:

  • Collaborate with functional project teams in a matrix environment to drive team accountability for quality deliverables;
  • Represent Quality on cross-functional Teams and participates in site initiatives and projects;
  • Review of analytical and technical documentation and independently manage complex method and product issues;
  • Review of analytical method transfer documentation package (transfer plans and reports, gap assessments, deviations);
  • Applies scientific and engineering principals for problem solving and advise to the teams;
  • Safeguards effective interfaces and dependencies with other programs and compliance with technical standards;
  • Challenges the status-quo. Involved in conception of new ideas, leads process improvements and contributes to the ongoing development of new procedures, techniques and departmental guidelines;
  • Complies to EHS and GMP-standards and has solid JnJ Credo awareness acting accordingly


Dexter van der Swaluw


Stuur uw cv naar onder vermelding van vacature id (856)

Meer informatie?

Neem contact op met Dexter van der Swaluw van ons kantoor te Zoetermeer, te bereiken op nummer +31 6-82436608