Director Clinical Quality Assurance Compliance

London, United Kingdom; Mainz, Germany | full time

As Director Clinical Quality Assurance Compliance you will lead quality assurance activities across clinical development programs in global teams. This role focuses on implementing a proactive, risk-based quality strategy, ensuring GCP compliance, fostering a culture of quality within the Global Development Organization whilst supporting delivery of our clinical trial portfolio.

Your Main Responsibilities Are

• Develop and implement a proactive, risk-based Clinical Quality Strategy for assigned high-priority trials or programs, ensuring inspection readiness and GCP compliance
• Collaborate with internal teams, collaboration partners as well as external vendors (e.g. CROs) to identify, investigate, and remediate clinical trial risks and quality issues, including CAPAs and effectiveness checks
• Actively contribute to Clinical Trial teams by providing quality guidance and reviewing key study documentation
• Enable continuous inspection readiness and compliance with GCP, regulatory requirements, and internal standards
• Lead or support inspection preparation, facilitation, and follow-up activities
• Review and manage Quality Agreements with CROs and other vendors, ensuring compliance with agreed standards
• Lead and develop a team, fostering transparency and proactive communication
• Drive a culture of quality and continuous improvement across the Global Development Organization, including authoring and reviewing clinical quality procedures
• Acting as an ambassador for quality: ensuring that quality is an enabler of delivery

What You Have to Offer

• University degree in life sciences; advanced degree preferred
• Profound professional experience (beyond 10 years) in a GCP-regulated environment
• Strong GCP expertise gained in a senior Quality Management and / or Clinical Operations role
• Strategic and Risk-based mindset with experience developing quality strategies at program level
• Solid understanding of global clinical regulations and guidelines (ICH, FDA, EMA, MHRA)
• Experience in team leadership and development (in the GCP environment preferred)
• Experience in managing, hosting or supporting regulatory authority inspections (EMA/FDA/MHRA)
• Proficiency in MS Office and electronic quality management systems
• Fluent in English (German is a plus)

Your Benefits:

BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate's qualifications and experience.

BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer.

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