Management Review Lead

Job description

The Management Review Lead is responsible for shaping Management Review into a forward-looking, insight-driven governance process that connects quality system performance with patient safety, portfolio risk, and enterprise decision-making.

The role provides senior leadership with a clear, predictive, and actionable view of quality health, enabling proactive risk management and continuous improvement of the Pharmaceutical Quality System across the product lifecycle.

This position supports the evolution of Management Review from “what happened” to “what matters next.”

- Review and challenge Management Review inputs and reports

- Design and evolve an end-to-end Management Review framework across global, functional, and site levels

- Ensure alignment with ICH Q10, with a strong focus on decision effectiveness

- Translate complex QMS data into clear executive insights, highlighting trends, risks, and early warning signals

- Support senior leaders with quality risk prioritization and informed decision-making

- Ensure decisions are documented, outcome-driven, and followed through

- Continuously improve Management Review maturity using benchmarks and internal learning

- Embed lessons learned from inspections, recalls, and external quality events

- Position Management Review as a demonstrator of quality culture during audits and inspections

Criteria

- Solid experience executing Management Review processes (data preparation, documentation, meeting support, action tracking)

- Strong expertise in pharmaceutical Quality Management Systems, governance, and quality risk management

- Ability to synthesize complex data into clear, actionable insights for senior leadership

- Strong strategic mindset with a focus on patient safety and business impact

- Data-driven, with experience identifying trends, leading and lagging indicators, and systemic risks

- Comfortable influencing across functions and at executive level

- Strong communication skills and confidence in challenging constructively

- Passion for patient-centric quality decision-making

- Experience with global governance forums, inspections, or major quality events is a plus

Offer

- Attractive salary in line with the market and your experience;

- Salary package with very competitive extra-legal benefits;

- Optimum work-life balance thanks to 12 ADV days, sliding hours and homeworking possibilities;

- Join a community of over 180 consultants in quality and regulatory affairs, with many social events organized throughout the year;

- Training and workshops to develop/share your skills.