Qualification & Validation Engineer

  • Randstad
  • 3500.00 - 4500.00
  • 32-40 hours
  • Bachelor degree

Client

Our client is a leading project management and engineering company for industry around the world.

Client

Our client is a leading project management and engineering company for industry around the world. Their reputation is based on forming successful partnerships with their customers, offering them innovative designs and cost-effective solutions in the context of sound judgment, strong management and technical excellence. They offer Full Service Engineering for their customers, including project and program management, purchasing, design, construction management, health and safety management, commissioning, qualification and start-up for numerous projects in various market sectors.

Requirements

  • BSc degree in a relevant area.
  • GMP experience in pharmaceutical or relevant industries required.
  • Qualification and Validation experience required.
  • Preferably experience with cleanrooms.
  • Fluent in English both verbally and in writing
  • Good communication skills and ability to work in teams under high pressure.

What do you get?

  • 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

Duties

  • Create and execute qualification protocols (IOQ / PQ), including identification and resolution of non-conformances/deviations.
  • Oversee and manage validation instrument inventory including calibrations.
  • Review technical documentation including protocols and summary reports for IOQ / PQ testing, and validation.
  • Perform temperature mapping and other miscellaneous validation activities.
  • Manage contractors performing equipment and system qualifications.
  • Report status and progress of qualification activities or projects.
  • Perform investigations and implement corrective actions related to CAPA’s and deviations.
  • Develop technical specifications and support the execution of engineering projects.

TAGCLOUD

pharma
#CQV
#validation
#qualification
#engineer
#GMP
#cleanroom
Peter Debrichy

Interested

Send your resume to peter@tailorminds.com referring to job id (1239)

More information?

Please contact Peter Debrichy working at our office in Zoetermeer, phone number +31 6-10191580

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