Global C&Q Director: Lead Global Validation & Compliance

The Association of Technology, Management and Applied Engineering; Brentford, Barnard Castle, Irvine; Hybrid; GBP 90,000 - 120,000; Full time

Job summary

A leading biopharma company is seeking a Global C&Q Director to drive strategies and manage the execution of commissioning and qualification projects. You will ensure that all systems and processes meet rigorous regulatory standards, collaborating with various teams to enhance operational compliance. The ideal candidate will possess an engineering degree, extensive project management experience, and the ability to lead diverse teams towards common goals. This role offers a hybrid working model based in the UK.

Qualifications

• Extensive project validation experience in pharmaceutical or biotech industry.
• Proven track record of managing regulatory audits.
• Strong understanding of the capital project lifecycle.

Responsibilities

• Lead global C&Q strategies, policies, and procedures.
• Oversee planning and execution of C&Q projects.
• Ensure compliance with regulatory standards.

Skills

Leadership skills

Project management skills

Technical expertise

Stakeholder management

Regulatory compliance knowledge

Education

Engineering degree (Mechanical, Electrical, Chemical, Civil/Structural)

Job description

A leading biopharma company is seeking a Global C&Q Director to drive strategies and manage the execution of commissioning and qualification projects. You will ensure that all systems and processes meet rigorous regulatory standards, collaborating with various teams to enhance operational compliance. The ideal candidate will possess an engineering degree, extensive project management experience, and the ability to lead diverse teams towards common goals. This role offers a hybrid working model based in the UK.