Quality Compliance Expert.

job details

summary.

  • specialism
    administration
  • contact
    Nils Bellieres
  • reference number
    129085-40326

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job details

As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:

Pharmaceutical Quality System (PQS): ensure maintenance of the Pharmaceutical Quality System (PQS) at site level:

  • Day-to-day operations by maintaining knowledge of company policies, SOPs, and supporting documents
  • Ensure compliance of local Pharmaceutical Quality System with the company Quality standards by ensuring that all documents are communicated and timely implemented across the site
  • Ensure robust process for local PQS management
  • Ensure monitoring at site level, support Quality and Performance metrics
  • Issue related periodic reports when appropriate.

Documentation management

  • Coordinate local Community of Practices
  • Ensure periodic review monitoring
  • Administrate active BCP once it's activated.
  • Act as key user for the documentation management system (DMS)

Training:

  • Provide Training on GMP related topic
  • Issuance of E-Learning
  • SpeachMe administrator

Projects:

  • Process improvement of areas under your responsibilities
  • Implementation new e-QMS

As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:

Pharmaceutical Quality System (PQS): ensure maintenance of the Pharmaceutical Quality System (PQS) at site level:

  • Day-to-day operations by maintaining knowledge of company policies, SOPs, and supporting documents
  • Ensure compliance of local Pharmaceutical Quality System with the company Quality standards by ensuring that all documents are communicated and timely implemented across the site
  • Ensure robust process for local PQS management
  • Ensure monitoring at site level, support Quality and Performance metrics
  • Issue related periodic reports when appropriate.

Documentation management

  • Coordinate local Community of Practices
  • Ensure periodic review monitoring
  • Administrate active BCP once it's activated.
  • Act as key user for the documentation management system (DMS)

Training:

  • Provide Training on GMP related topic
  • Issuance of E-Learning
  • SpeachMe administrator

Projects:

  • Process improvement of areas under your responsibilities
  • Implementation new e-QMS

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NB

Nils Bellieres

  • Randstad Merck Aubonne

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