Lab Equipment Specialist

  • Randstad
  • 3500.00 - 4500.00
  • 32-40 uren
  • HBO

Opdrachtgever

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

Opdrachtgever

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.

functie Vereisten

  • Bachelor or Master degree with technical background.
  • 4 to 5 years experience in the pharmaceutical industry or an equivalent GMP environment.
  • Experience with validation of laboratory equipment.
  • Team player with sound communication skills and pro-active approach.
  • Good knowledge of laboratory equipment with experience in calibration, qualification and validation.
  • Experience with deviations, changes and CAPA writing.
  • Support laboratory investigations as equipment SME.
  • Knowledge of Empower CDS (in combination with (U)HPLC and GC), particle analysis and basic analytical instruments is a pre.

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

Werkzaamheden

  • Assess qualification (incl. validation) and implementation of (computerized) Laboratory equipment.
  • Oversee the timely completion of all validation documentation, including coordination of contractor activities.
  • Support the regulatory defense of validation protocols and summary reports during audits and internal audits.
  • Write training instructions, calibration ,maintenance , operational procedures, equipment specification files and reports ((URS, Risk assessments, IQ/OQ/PQ).
  • Fulfill the role of a Subject Matter Expert and participate actively during audits.
  • Being person of contact between suppliers and laboratory.
  • Develop Validation Master Plans, Validation Project Plans and Project Schedules as needed.

TAGCLOUD

validation
#qualification
#laboratory
#GMP
#pharma
#equipment
#validationmasterplan
#URS
Peter Debrichy

Geïnteresseerd?

Stuur uw cv naar peter@tailorminds.com onder vermelding van vacature id (1202)

Meer informatie?

Neem contact op met Peter Debrichy van ons kantoor te Zoetermeer, te bereiken op nummer +31 6-10191580

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