Global VP Quality: GMP Mastery & Regulatory Strategy

Prothya Biosolutions Netherlands B.V; Amsterdam; Hybrid; EUR 180,000 - 260,000; Full time

Job summary

Prothya Biosolutions Netherlands B.V. is seeking a Vice President Quality to shape and drive the global quality strategy across all sites, including Amsterdam and Brussels.

In this senior role you will ensure GMP/regulatory compliance, lead Quality Systems, CAPA, audits, risk management and validation, and mentor a high-performing team. Fluent English is essential; additional languages are an advantage.

Qualifications

• Master’s degree in Life Sciences, Pharmacy, or related field; PhD is a plus.
• Minimum 15 years of experience in Quality within biopharmaceutical industry, with at least 8 years in senior leadership.
• Deep knowledge of GMP, regulatory requirements, and quality systems.
• Proven track record in managing global teams and complex projects.
• Strong leadership, communication, and stakeholder management skills.
• Fluent in English; additional languages are an advantage.

Responsibilities

• Develop and implement the global Quality strategy aligned with corporate objectives.
• Ensure compliance with GMP, EMA, FDA, and other relevant regulatory standards.
• Oversee Quality Systems, including CAPA, audits, risk management, and validation.
• Lead and mentor a high-performing Quality team across multiple sites (Amsterdam, Brussels, and other locations).
• Act as the primary contact for regulatory authorities during inspections and audits.
• Drive continuous improvement initiatives to enhance efficiency and compliance.
• Collaborate with senior leadership to integrate quality into business decisions.

Skills

GMP knowledge

Regulatory compliance

Quality systems

Leadership

Stakeholder management

English fluency

Education

Master’s degree in Life Sciences, Pharmacy, or related field

PhD (advantage)

Job description

Prothya Biosolutions Netherlands B.V. is seeking a Vice President Quality to shape and drive the global quality strategy across all sites, including Amsterdam and Brussels.

In this senior role you will ensure GMP/regulatory compliance, lead Quality Systems, CAPA, audits, risk management and validation, and mentor a high-performing team. Fluent English is essential; additional languages are an advantage.