Qualification/Validation Corporate Manager

Barrington James Limited; Cholet; Sur place; EUR 45 000 - 75 000; Plein temps

Résumé du poste

Une entreprise innovante recherche un Responsable Qualification/Validation Corporate expérimenté pour rejoindre son équipe. Ce rôle passionnant exige une expertise en qualité dans les environnements industriels, particulièrement dans les secteurs cosmétique et pharmaceutique. Vous serez chargé de développer des stratégies de validation, de gérer des activités de qualification et de collaborer avec des équipes interfonctionnelles pour garantir la conformité aux normes de qualité. Si vous êtes proactif et possédez une solide connaissance des pratiques de fabrication, cette opportunité est faite pour vous.

Qualifications

• 5+ années d'expérience en qualité dans un site industriel, idéalement cosmétique ou pharmaceutique.
• Connaissance approfondie des pratiques de fabrication et des normes de qualité.

Responsabilités

• Développer et mettre en œuvre des stratégies de validation et de qualification.
• Gérer les activités de validation et qualification des processus de fabrication.

Connaissances

Compétences interpersonnelles

Proactivité

Connaissance des GMP

Normes de qualité (ISO)

Formation

Master en Qualité

Master en Ingénierie de la Qualité

Master en Pharmacie Industrielle

Outils

Microsoft Office Suite

Description du poste

Overview

We are seeking a highly skilled and experienced Qualification/Validation Corporate Manager to join our team. The ideal candidate will have a Master's degree in Quality, Quality Engineering, or Industrial Pharmacy with at least 5 years of experience in quality within an industrial site, ideally in cosmetic and pharmaceutical environments. The candidate should demonstrate strong interpersonal skills, proactivity, proficiency in office tools, and a deep understanding of GMP and quality standards.

Responsibilities

• Develop and implement validation and qualification strategies to ensure compliance with regulatory requirements and industry standards.
• Lead and manage validation and qualification activities for new and existing manufacturing processes, equipment, and facilities.
• Collaborate with cross-functional teams to ensure that validation and qualification activities align with business objectives.
• Review and approve validation and qualification documentation, including protocols, reports, and risk assessments.
• Provide guidance and support to internal teams on validation and qualification best practices and standards.
• Stay informed about industry trends and regulatory changes related to validation and qualification.

Qualifications

• Master's degree (Bac+5) in Quality, Quality Engineering, or Industrial Pharmacy.
• Minimum of 5 years of experience in quality within an industrial site, preferably in cosmetic and pharmaceutical environments.
• Strong interpersonal skills and proactivity.
• Proficiency in office tools (Microsoft Office Suite).
• Deep knowledge of GMP (Good Manufacturing Practices) and quality standards (ISO, etc.).

Day-to-day

• Collaborating with cross-functional teams to ensure validation and qualification activities align with business objectives.
• Reviewing and approving validation and qualification documentation.
• Providing guidance and support to internal teams on validation and qualification best practices and standards.
• Staying informed about industry trends and regulatory changes related to validation and qualification.