QA Manager, Gmp

il y a 2 jours

Lyon, France Proclinical Staffing Temps plein

**Responsibilities**:

- Maintain and improve the Quality Management System (QMS) in line with regulatory standards.
- Document and enhance QA processes and procedures.
- Conduct audits and participate in regulatory inspections.
- Ensure product compliance with regulations and implement new requirements.
- Prepare and review quality-related documentation and reports.
- Conduct risk assessments and manage quality issues.
- Oversee the CAPA process and manage change control.
- Provide training and development in QA processes.
- Collaborate with cross-functional teams to ensure product quality.
- Lead initiatives for process improvements and quality enhancement.

**Key Skills and Requirements**:

- Degree in pharmacy or related field preferred.
- Experience with GMP in manufacturing, understanding of CMOs.
- Strong knowledge of Good Manufacturing Practices.
- Experience in quality management systems and regulatory inspections.
- Excellent communication skills; proficiency in English required, other languages a plus.
- Ability to manage multiple projects in a fast-paced environment.
- Certification in quality assurance is a plus.
- Willingness to travel to CMO partners.
- Agile thinker, problem solver, and team player with a growth mindset.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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