Chief Quality Officer (Small molecule CDMO)

KinetiQ Life Sciences; Plasencia; In loco; EUR 80.000 - 120.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a Chief Quality Officer to lead the global Quality function within their CDMO operations. This pivotal role requires a visionary leader who can drive a culture of quality, ensure regulatory compliance, and enhance customer satisfaction across all development and manufacturing sites worldwide. With over 20 years of experience in the pharmaceutical industry, the ideal candidate will bring a wealth of knowledge and a proven track record in quality leadership. If you are passionate about making a significant impact in a dynamic environment, this opportunity is perfect for you.

Competenze

• 20+ years of experience in quality roles within the pharmaceutical industry.
• Demonstrated track record in a CDMO environment preferred.

Mansioni

• Provide strategic quality leadership across global operations.
• Oversee regulatory compliance and inspection management.

Conoscenze

Quality Leadership

Regulatory Compliance

Client Management

Strategic Oversight

Formazione

MSc in Chemistry

PhD in Life Sciences

Descrizione del lavoro

Chief Quality Officer (Small molecule CDMO)

KinetiQ Life Sciences

The Chief Quality Officer (CQO) will serve as a critical member of the Executive Leadership Team, providing visionary leadership and strategic oversight for the global Quality function across the organisation’s CDMO operations. This role will be responsible for driving a culture of quality, ensuring regulatory compliance, enhancing customer satisfaction, and delivering consistent quality performance across all development and manufacturing sites worldwide.

Job responsibilities:

1. Provide strategic quality leadership
2. Oversight of global quality operations
3. Overseeing regulatory compliance and inspection management
4. Deliver client-facing quality leadership

Job requirements:

1. MSc or PhD in Chemistry or related Life Sciences discipline
2. 20+ years experience in quality roles within pharmaceutical industry
3. Demonstrated track record in a CDMO environment preferred
4. Fluent in both Italian and English required