Chief Quality Officer (Small Molecule Cdmo)

Buscojobs; Campania; In loco; EUR 80.000 - 150.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a Chief Quality Officer to lead its global Quality function across CDMO operations. This pivotal role requires a visionary leader with over 20 years of experience in the pharmaceutical industry, particularly in quality roles. The CQO will drive a culture of quality, ensuring compliance and enhancing customer satisfaction across all development and manufacturing sites. Fluency in both Italian and English is essential for effective communication in this dynamic environment. Join this innovative firm to make a significant impact on quality performance worldwide.

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 for global operations.
• Oversee regulatory compliance and inspection management.
• Deliver client-facing quality leadership.

Conoscenze

Regulatory Compliance

Quality Leadership

Client Management

Fluency in Italian

Fluency in English

Formazione

MSc in Chemistry

PhD in Life Sciences

Descrizione del lavoro

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 the pharmaceutical industry
3. Demonstrated track record in a CDMO environment preferred
4. Fluent in both Italian and English required