Quality Assurance Auditor GLP

  • Drenthe
  • 3000.00 - 4000.00
  • 32-40 uren
  • HBO

Opdrachtgever

Our client is a world-leading healthcare intelligence and clinical research organisation.

Opdrachtgever

Our client is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. They help to accelerate the development of drugs and devices that save lives and improve quality of life.

functie Vereisten

  • Life science degree (Bachelor or Master) from an accredited institution
  • Previous experience working as a GLP Auditor
  • Additional experience on any of the following topics is considered a pro: Data Integrity and CSV
  • Work experience in a bioanalytical laboratory is considered an additional benefit
  • Fluency in Dutch and English
  • You are a self-motivated, focused individual with excellent communication skills

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

We are looking for you to join the GLP team where you will take responsibility for Bioanalytical Laboratory study audits and parts of the clients audit program. Your responsibilities will include and will not be limited to:

  • Perform routine and complex study, vendor and process audits according to GxP regulations, scientific guidelines, client expectations and/or PRA SOPs.
  • May function as a lead auditor on an (international) audit team.
  • Ensure planning, conduct, reporting, responses and FU actions are managed according to internal procedures
  • Further aspects of this challenging role include the interpretation of regulations and guidance documents governing Bioanalytical studies (GLP, GCP, EMA etc) and applying this within day-to-day structures for PRA staff and client representatives.
  • You will be additionally responsible for facilitating client audits and regulatory inspections at PRA.

TAGCLOUD

Bas Lokhorst

Geïnteresseerd?

Stuur uw cv naar bas@tailorminds.com onder vermelding van vacature id (998)

Meer informatie?

Neem contact op met Bas Lokhorst van ons kantoor te Zoetermeer, te bereiken op nummer +31 6 82 43 66 08

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