Qualification/Validation Corporate Manager

Barrington James Limited; Angers; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading quality-focused company in France is seeking a highly skilled Qualification/Validation Corporate Manager. You will develop and implement validation strategies and lead qualification activities in compliance with industry standards. The ideal candidate has a Master's degree and at least 5 years of experience in quality within cosmetic and pharmaceutical environments, demonstrating strong interpersonal skills and a deep understanding of GMP. This role offers an opportunity to collaborate with cross-functional teams in a dynamic environment.

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.
• Strong interpersonal skills and proactivity.

Responsabilités

• Develop and implement validation and qualification strategies.
• Lead and manage validation and qualification activities.
• Collaborate with cross-functional teams to align activities with business objectives.

Connaissances

Interpersonal skills

Proactivity

Proficiency in office tools

Deep understanding of GMP

Formation

Master's degree in Quality, Quality Engineering, or Industrial Pharmacy

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