Quality Systems Officer

  • Brabant
  • 3750.00 - 4250.00
  • 32-40 hours
  • Bachelor degree

Client

Our client is a leading Project Management and Engineering company serving the pharmaceuticals industry around the world.

Client

Our client is a leading Project Management and Engineering company serving the pharmaceuticals industry around the world. Their reputation is based on forming successful partnerships with clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.

Requirements

  • At minimum a bachelor’s degree (Dutch: HBO/HLO), preferable in Science.
  • At least 5 years of relevant experience in the pharmaceutical industry and cGMP.
  • Applied knowledge of relevant Quality and Compliance guidelines.
  • Excellent interpersonal and communication skills, oral and written (Dutch and English).
  • Experience with document/quality management systems such as Trackwise® and SAP is preferable.
  • Preferably Lean Six Sigma Yellow/Green belt trained.

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

  • Responsible for execution of all internal system audit activities which are in line with relevant quality procedures, guidelines.
  • Monitor the status of GMP level.
  • Responsible for preparation, execution and follow-up on inspections.
  • Responsible that all relevant documents are in line with relevant quality procedures, guidelines to ensure full compliance.
  • Responsible for providing advice/guidance to the functional areas on quality knowledge, procedures, guidelines and directives
  • Responsible for supporting Continuous Improvement.
  • Leads the Quality Risk Management efforts.
  • Provides day to day support for operations, raising concerns if needed or directing users to do so.
  • Responsible for the support of training initiaties and activitely contribute in the overall and current GMP knowledge of all personell.
  • Responsible for Compliance and Quality Agreement of departments, customers and inter-site activities.

TAGCLOUD

qualitysystems
#GMP
#QA
#pharma
#compliance
#qualityassurance
Peter Debrichy

Interested

Send your resume to peter@tailorminds.com referring to job id (1514)

More information?

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

APPLY USING THE FORM BELOW

  • Max. file size: 64 MB.
  • Hidden
  • Hidden
  • This field is for validation purposes and should be left unchanged.