
Secteur d'activité
Industries
Niveau de poste
Manager / Responsable Département
Niveau d'étude (diplome)
Master 2, Ingéniorat, Bac + 5 | Magistère Bac + 7 | Doctorat
Date d'expiration
04 janvier 2027
Nombre de postes
1 poste ouvert
Type de contrat
CDI
Années d'expérience
6 À 10 Ans
Qualifications & Experience
Bachelor's degree in Chemistry, Pharmacy, Chemical Engineering, or a related scientific field.
Minimum 7 years of experience in Quality Assurance, preferably in pharmaceutical or analytical laboratory environments.
At least 3 years of experience in a QA managerial role.
Strong practical experience in ISO/IEC 17025, including QMS implementation, internal audits, and accreditation requirements.
Good knowledge of pharmaceutical GMP requirements and general pharmaceutical Quality Assurance practices.
Experience in quality management systems, including SOPs, documentation control, deviations, CAPA, change control, and risk management.
Experience in analytical laboratory quality systems, method validation, equipment qualification, and data integrity.
Ability to establish, implement, and maintain quality systems across laboratory and pharmaceutical manufacturing operations.
Strong leadership, problem-solving, and communication skills.
Proficiency in French and English.
Additional Advantages (Preferred, Not Mandatory)
Knowledge of ISO 17034 requirements for reference material producers.
Familiarity with Reference Standards / Certified Reference Materials production and quality requirements.
Experience in pharmaceutical raw material manufacturing or pilot-scale production.
Previous experience establishing a QMS or preparing a facility for accreditation.
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