Société : Alten Lieu : Brussels Brussels Site source : Talent BE
Ensuring correct implementation and follow-up of CAPAs.Reviewing SOPs, educational tools, batches, and other GMP-related documents.Contributing to improving the content and process of the quality system.Developing solutions to reduce quality-related risks.Assessing changes within the change control framework.
QualificationsMaster’s degree in Bioengineering, Industrial Pharmacy, or related fields.Eligibility for the V.I.E program.Experience in quality systems (non-conformance, compliance, etc.) and GMPs.Knowledge of production processes and QA in the pharmaceutical industry.Proficiency in both English and French.
Informations supplémentairesEngineering culture and passion for technology, high value-added projects, mobility offers and personalized career follow-up, it is in an innovative and stimulating environment that our teams mobilize to:
Innovate:
become an actor of the digital transformation by taking part in innovative technological projects within a technological environment based on creativity, innovation and the search for solutions.
Evolve:
ALTEN is a career gas pedal that allows you to grow quickly and according to your desires.
Benefit from dedicated support, with the possibility of training and certification, to develop your expertise and grow within our four areas:
Specialists, Project Management, Business Management and Support Functions.
Grow:
work in an agile group that values the talents of each individual and join a company that is committed:
ALTEN develops and finances citizen and solidarity partnerships and offers its employees the opportunity to get involved in these projects. Alten BrusselsBrussels
