About this role

  • Posted on

  • Location

    Liege

  • Salary

    Up to £0.00 per annum

  • Type

    Permanent

  • Division

    Pharmaceutical Quality Assurance Jobs

  • Reference

    BBBH18434UK_1619626042

  • Start date

    ASAP

  • Managing this role

Consultant

Urszula Kaldi

+44 (0) 203 8543 089

urszula.kaldi@xplorepharma.com

154-158 Shoreditch High Street

Description

Responsibilities

  • Ensure quality oversight of the Qualification/Validation & Environmental monitoring project activities and participate in key meetings and decision making
  • Review and approve documentation related to qualification/validation of production equipment and environmental monitoring
  • Support, review and approve POL/SOP/WKI write-up for related activities
  • Ensure quality system application, maintenance and periodic review (deviation, CAPA, risk, change control, documentation )
  • Actively participate in continuous improvement of plant activities
  • Escalate any quality risks / issues to higher QA management
  • Participate in internal audit program and CAPA follow-up, inspection/audits by authorities and customers, and ensure inspection/ audit readiness
  • Take part, review, support and approve investigations related to deviations and CAPAs with a solution driven perspective
  • Follow training as needed to fulfill function requirements, and provide quality training to the team

Requirements

  • 8-10 years experienced in QA Qualification/Validation
  • Bachelor or Master in a Scientific Area
  • Good knowledge of GMP
  • Good knowledge in English
  • Previous experience working in pharmaceutical/ biotech industry.

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