Quality Assurance Director
Il y a 5 mois
**Role**:Quality Assurance Director - GMP Quality
**Location**:Paris, France
At Stirling Q&R, we are excited to present an exceptional opportunity for a Quality Assurance Director - GMP Quality with one of our esteemed clients in the pharmaceutical industry. As a specialist Quality & Regulatory headhunting company for the life sciences, we are dedicated to connecting top talent with organizations that value excellence, compliance, and innovation.
**About Our Client**:
Our client is a visionary pharmaceutical company that stands at the forefront of medical innovation. With a strong commitment to improving patient lives through cutting-edge therapies, they have positioned themselves as leaders in the industry. This company prides itself on fostering a culture of quality, compliance, and continuous improvement, making them an ideal workplace for professionals who share their passion for advancing healthcare.
As the Quality Assurance Director - GMP Quality for our client, you will hold a pivotal role in upholding their commitment to the highest standards of quality and compliance within the pharmaceutical industry. Your strategic leadership and expertise will ensure that their GMP processes meet and exceed regulatory expectations, contributing significantly to the overall success of the organization.
**Responsibilities**:
- Lead and manage the Quality Assurance team, offering guidance, mentorship, and strategic direction.
- Develop, implement, and maintain a robust Quality Management System (QMS) to ensure adherence to GMP regulations and industry best practices.
- Oversee the quality aspects of product lifecycle management, from development to commercialization, ensuring compliance at all stages.
- Collaborate cross-functionally to instill a culture of quality throughout the organization, promoting continuous improvement and effective risk management.
- Serve as the main point of contact for regulatory inspections, audits, and compliance matters, ensuring successful outcomes.
- Provide leadership in identifying and resolving quality-related issues, deviations, and CAPA management.
- Stay updated on evolving regulatory requirements and industry trends, integrating them into the QMS as needed.
**Requirements**:
- Bachelor's or advanced degree in a relevant scientific field.
- Extensive experience (10+ years) in Quality Assurance within a GMP-regulated pharmaceutical environment.
- Strong working knowledge of GMP regulations (e.g., EU, FDA), quality systems, and industry standards.
- Proven track record in managing and leading quality teams to achieve operational excellence.
- Exceptional communication, leadership, and problem-solving skills.
- Fluency in English (additional languages are a plus).
- Ability to foster a collaborative and compliance-oriented environment.
**Why Apply**:
By joining our client's team, you will contribute to their ongoing success in a role that offers both challenge and fulfilment. Your expertise will shape their quality strategy, impact patient lives, and drive innovation within the pharmaceutical sector. With a competitive compensation package, professional growth opportunities, and a dynamic team, your contributions will be valued and celebrated.
**Application Process**:
**Salary**: 110,000.00€ - 150,000.00€ per year
Ability to commute/relocate:
- Paris (75): Reliably commute or planning to relocate before starting work (required)
**Experience**:
- Quality Assurance: 10 years (preferred)
- Pharmaceutical: 10 years (preferred)
Work Location: In person
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