Chief Quality Officer (Small molecule CDMO)

JR Italy; Palermo; In loco; EUR 80.000 - 150.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a Chief Quality Officer to lead the Quality function across global CDMO operations. This pivotal role involves driving a culture of quality, ensuring compliance with regulatory standards, and enhancing customer satisfaction. With over 20 years of experience in quality roles, the ideal candidate will provide strategic oversight and leadership, ensuring consistent quality performance across all sites. This is a unique opportunity to make a significant impact in a dynamic environment, where your expertise will shape the future of quality in the pharmaceutical industry.

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

Strategic Quality Leadership

Regulatory Compliance

Client Facing Quality Leadership

Quality Operations Oversight

Formazione

MSc in Chemistry

PhD in Life Sciences

Descrizione del lavoro

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Chief Quality Officer (Small molecule CDMO), palermo

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Client:

KinetiQ Life Sciences

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

65312317834788864337141

Job Views:

2

Posted:

26.04.2025

Expiry Date:

10.06.2025

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Job Description:

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:

• Provide strategic quality leadership
• Oversight of global quality operations
• Overseeing regulatory compliance and inspection management
• Deliver client facing quality leadership

Job requirements:

• Msc or PhD in Chemistry or related Life Sciences discipline
• 20+ years experience in quality roles within pharmaceutical industry
• Demonstrated track record in a CDMO environment preferred
• Fluent in both Italian and English required