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Agence de traductionJobsCDIQuality Assurance Specialist

Quality Assurance Specialist

Bruxelles — CDI

À propos

Acolad is one of the leading European language service providers and the most dynamic business in its industry. The group has a presence in 14 countries on 3 continents and distinguishes itself by its multi-local market approach, a rare trait which has made it the preferred partner of many clients around the world.

Acolad has a strong footprint in the field of Life Sciences, particularly Clinical Trials, and is looking for a Quality Assurance Specialist based in Brussels to reinforce the team locally and to contribute to the Quality Assurance effort at group level.

 

 

 

 

 

 

Key Responsibilities

As a QA Specialist, you will be responsible for managing QA activities for Acolad Brussels, particularly for the Life Sciences division. You will report to the General Manager while working closely with the Head of Quality Management for the group.   

  • Develop and implement processes, procedures, work instructions and tools related to quality systems/processes ;
  • Write or review Standard Operating Procedures (SOPs) in accordance with GCP requirements;
  • Maintain Acolad’s QMS and Quality Assurance documentation;
  • Develop standard measurements against which processes will be compared, inspected and tested;
  • Participate in handling customer complaints ;
  • Investigate deviations and non-conformities;
  • Initiate and ensure follow-up on CAPA (Corrective Action Preventive Action) - risk assessment, root cause assessment deviation assessment etc. ;
  • Coordinate Internal/External audits;
  • Provide support and direction to all departments to ensure that business, quality and compliance goals are met ;
  • Train and provide assistance to QA and other teams on quality procedures and documentation;
  • Research and advise Acolad on recent regulatory changes and their impact on our business and that of our clients
  • Guide and support other entities within Acolad on quality assurance topics, particularly Life Sciences.

Your profile

 

  • Perfect command of English and French; (an additional language is a plus);
  • A minimum of 2 years’ experience in a quality, validation or compliance role within the pharmaceutical industry ;
  • Knowledge of FDA/EMEA regulatory requirements applicable to pharmaceuticals ;
  • Knowledge of GDPR requirements applicable to the pharmaceutical industry/Clinical Trials ;
  • Ability to apply GCP regulations and other FDA and international guidelines to all aspects of the position ;
  • Experience in QMS development in compliance with GCP is desirable ;
  • IT-minded, team-spirited, rigorous, high sense of responsibility, organization and priorities ;
  • Ability to work autonomously while remaining a valuable member of an efficient team.

We offer you

  • A permanent employment contract;
  • Competitive salary package;
  • A growing international company with a multicultural environment;
  • Great location in Ixelles with easy access to public transport  : 200 meters from Vleurgat (tram line 8 or 93) ;
  • Meal vouchers, hospitalization and health insurances

Interested?

Send your resumé along with a motivation letter to our Human Resources Department recruitment@telelingua.com with this reference in your subject:  « QA 09/2020 »

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