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Senior Quality Assurance Officer

  1. Amsterdam
Netherlands
  1. Contract
Competitive
  1. Compliance / Quality Assurance
18-09-2020
AE25461

This vacancy has now expired

Do you want to be involved with exciting Pharmaceutical projects?

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Senior Quality Assurance Officer.

This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.

ABOUT THE POSITION

As a (Senior) Quality Assurance Officer you are responsible for checking the general cGMP compliance of our production location in the Netherlands, suppliers and contract laboratories. These checks are carried out on the basis of internal guidelines, procedures, experience and interpretation of general laws and regulations. As a Quality Assurance Officer you participate in multidisciplinary projects as a representative of Quality.

PRIMARY RESPONSIBILITIES

As a (Senior) Quality Assurance Officer, reporting to the QA Lead, you are responsible for:
  • Reviewing, advising and checking validation projects within the site. Within these projects you are the representative of Quality.
  • Guaranteeing the validated status of cGxP processes, subsystems and suppliers.
  • Fulfilling the Quality role in technical projects, both process and IT.
  • Support and monitor the handling of deviations.
  • Checking and authorizing GMP documents, such as SOP's qualification / validation documentation and change control documentation.
  • Supporting CoEs and IPTs when introducing changes to guidelines.
  • Monitoring and auditing CoE and IPT activities with regard to compliance and taking the necessary actions. Performing audits as an internal Lead Auditor and supervising external audits.
  • Review and approve quality agreements with suppliers.
  • Coordinate and communicate complaints to exclusive suppliers of our production location and follow up the improvements at the same suppliers.

Your profile
  • HBO / WO pharmaceutical, process-technical or chemical background, supplemented with 3 years of relevant work experience in the field of quality;
  • You have gained this experience in a similar role as a QA officer;
  • You have experience with working under GMP and / or GDP;
  • Experience with packaging technology and / or production technology is an advantage;
  • Persuasiveness and result-oriented;
  • Accurate, flexible and independent;
  • Good communication skills in both word and writing in the Dutch and English language.
 
For further information and to have a confidential conversation please apply direct! 

The candidate must have the rights to work in the location stated in the job advert.

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