ALTEN is hiring a Quality Assurance Engineer to consult within the pharmaceutical industry, ensuring adherence to quality policy and objectives in line with Good Manufacturing Practices (GMP). You'll join a culture passionate about engineering and technology within an innovative and stimulating environment.
What You'll Do
- Write risk analyses.
- Participate in the investigation of deviations.
- Conduct internal audits.
- Ensure the correct implementation and follow-up of CAPAs.
- Review and approve documents related to operations (SOPs, training tools, batches, reports, and other GMP-related documents).
- Contribute to improving the content and process of the quality system.
- Develop solutions to reduce quality-related risks.
- Ensure the assessment of changes as part of change control.
What We're Looking For
- Master's degree in Bio-Engineering, Industrial Pharmacy, or a related field.
- Experience in quality systems (non-conformance, compliance, etc.) and in GMP.
- Knowledge of production processes and Quality Assurance in the pharmaceutical industry.
- Ability to work in English in addition to French.
Benefits & Compensation
- Personalized career tracking.
- Opportunity to complete training and obtain certifications.
- Chance to get involved in civic and solidarity partnerships.
ALTEN is committed to valuing the talents of each individual.
