Deputy RP

€4000 - €5000 per day
  1. Permanent
Anderlecht
  1. Quality Assurance
Posted: 17/03/2021
BBBH16141

This vacancy has now expired. Please see similar roles below...

A new opportunity has arisen for a Deputy RP to join an excellent pharmaceutical organisation in Belgium where you will help to proactively manage the lifecycle of the medicinal products.

Please note that to be considered for this role you must have the right to work in this location.


Job Responsibilities:

  • You will be the Deputy Responsible Person for the company.
  • To agree Quality agreements with external partners (contract manufacturers, logistic service providers and distributors).
  • Accountable to support in ensuring ongoing inspection readiness in the areas of responsibilities.
  • You support the internal and external audits.
  • To investigate quality incidents, deviations and complaints, identify and follow-up CAPA's and supplier improvement plans together with contract manufacturers and ensure all documentation is updated.
  • You evaluate and follow-up change controls as per company procedure.
  • You develop the Quality Communication Strategy for all levels of staff, to include written information, tool box talks and management briefs.
  • You support the maintenance of the Quality Management system as a SME.
  • You write Product Quality reviews.
  • Part of Supplier Qualification and regular Supplier Auditing.
  • To assist with integration of new product introductions.

Key Skills:

  • Self-starter and capable of working autonomously and are efficient.
  • A clear communicator, practical and solution orientated.
  • Change management skills.
  • You drive for performance (fast decision taking, positive, courage, curious, connected).
  • Seeks feedback to enhance performance.

Requirements:

  • A Master (in pharmaceutical sciences, engineering, biochemistry, chemistry,) or equivalent through professional experience.
  • At least 3 years of relevant experience in QA in the pharmaceutical industry.
  • Good knowledge of the relevant European regulations for manufacturing and distribution of pharmaceutical products and strong project management skills.
  • You speak and write Dutch, French and English. Other languages are an asset.
  • Occasional international travel is part of the role.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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