Head of Quality Braine Manufacturing

Make your mark for patients

To strengthen our Manufacturing Quality department we are looking for a talented profile to fill the position of: Head of Quality Braine Manufacturing – Braine l’Alleud, Belgium

About the role

The Head of Quality Braine Manufacturing is the senior Quality executive for one of UCB’s key manufacturing sites, with end-to-end accountability for Quality across commercial Drug Substance and Drug Product operations. The position leads the development of a unified, high-performing Quality organization, driving quality culture, operational excellence, continuous improvement, digital transformation, and organizational capability to support current operations and future business growth.

As a member of the Site Leadership Team and the Internal & Clinical Manufacturing Quality Leadership Team, the role actively contributes to site strategy, investment priorities, organizational capability and transformation. The position acts as a trusted partner and constructive challenger to Manufacturing and other site leaders, ensuring that Quality considerations are embedded in business decisions from strategy through execution.

You will work with

You will collaborate closely with Manufacturing and Site Leadership, as well as key partners across Supply, Technical Operations, MSAT, Regulatory, Engineering, HSE and External Manufacturing Quality. You will also work across the broader UCB Quality network and engage with regulatory authorities to ensure strong alignment on quality, compliance, operational performance and site priorities.

What you will do

Leadership & Management

Provide strategic leadership to the Braine Quality organization and serve as a key member of the Site Leadership Team, shaping site strategy, priorities, investment choices and long-term capabilities.

Create an empowered leadership team with clear accountability, strong collaboration and the capability to translate strategy into sustainable performance.

Develop people capability (technical, behavioral and managerial); ensure development plans, succession plans are in place to sustain the organization and retain key talent.

Foster a culture of quality, compliance and continuous improvement across Quality and Manufacturing on the site and within UCB.

Nurture strong top-down, bottom-up and transversal communication; promote continuous feedback and reduce variability to deliver One Quality Voice.

Own Quality workforce and financial planning and budget, ensuring resources and investments are aligned with strategic priorities and deliver sustainable value.

Quality Transformation & Future Readiness

Define and execute the strategic roadmap for the Braine Quality organization, aligned with site and UCB Quality priorities.

Lead the transformation toward a simpler, more agile and scalable Quality operating model that enables growth while maintaining strong compliance.

Accelerate adoption of digital, data, automation and AI capabilities to strengthen insight, decision-making, productivity and employee experience.

Challenge legacy ways of working and remove unnecessary complexity, ensuring Quality resources are concentrated on activities that create the greatest patient, compliance and business value.

Quality Assurance & Quality Systems

Ensure effective deployment and execution of global Quality Management System (QMS) processes and standards at site level, while driving harmonization and simplification

Organize adequate quality oversight of GMP documentation and activities; drive proactive deviation, investigation, CAPA and change control management supported by quality indicators.

Supervise quality governance for site operations and support functions; regularly review efficiency of the operating model with stakeholders Prepare product and process quality reports by collecting, analyzing and summarizing data and trends, to drive improvement.

Escalate significant/critical quality risks and issues to the right management levels per UCB QMS standards Chair the site Quality Management Review (ICH Q10) and own the site quality risk register; apply Quality Risk Management (ICH Q9(R1)) consistently in decisions.

Own the site Data Integrity program (ALCOA+)

Quality Operations & Release

Ensure the QP certification chain is robust across DS and DP

Collaborate closely with the External Manufacturing Quality organization that manages the starting materials, components, suppliers and vendors that are used on the site.

Maintain a robust and sustainable QP governance model, including formal succession, delegation, and competency frameworks, ensuring uninterrupted certification capability across products and operations.

Own quality aspects of the site manufacturing & import authorization(s) and GMP certificates; ensure variations and site-master-file updates are timely and accurate.

Ensure compliance with the Falsified Medicines Directive (safety features/serialization) for products certified at Braine

Quality Support, Validation & Sterility Assurance

Ensure site facilities, equipment, personnel, methods, processes and procedures conform to internal and regulatory standards.

Ensure Quality Support teams support projects (e.g., facility expansion) and lifecycle activities (periodic review, maintenance, calibration).

Ensure the validated state of facilities, utilities, equipment, processes, cleaning and computerized systems (Annex 11, Annex 15), including risk-based CSV/CSA.

Inspection Readiness & Regulatory Interactions

Act as primary liaison for regulatory inspections (foreign and domestic); direct all support and coordination and provide appropriate resources; own resulting improvement plans.

Represent the Braine site Quality organization in interactions with regulatory authorities, notably AFMPS, ensuring credibility, transparency, and proactive engagement on quality and compliance matters.

Ensure a single, operational site inspection-readiness program covering both DS and DP.

Ensure effective deployment of the Regulatory Intelligence Network (RIN) process within the organization, translating emerging regulatory requirements into timely impact assessments, implementation plans, and sustainable compliance strategies.

Product Protection, Crisis & Business Continuity

Lead quality decision-making for product complaints, quality events, market actions and recalls originating from the site, in line with UCB recall and crisis procedures.

Drive a proactive quality framework for quality risk management, operational resilience, and business continuity, ensuring the site can effectively respond to and recover from significant operational events (e.g., utility/HVAC failures, contamination events).

Projects, New Product Introduction & Growth

Support ramp-up, new product introductions and major project execution (e.g., expansion, digitalization).

Ensure quality oversight of technology transfers, process performance qualification and launch readiness, including pre-approval inspection readiness.

Monitor the quality organization design through growth phases and propose adjustments as required.

Continuous Improvement

Identify improvement opportunities and lead initiatives to enhance quality, compliance, efficiency, and organizational effectiveness across the value stream.

Establish and monitor a balanced set of quality and operational performance indicators, leveraging both leading and lagging metrics to proactively identify trends, risks, and improvement opportunities.

Drive right-first-time performance, cycle-time reduction, simplification, and waste elimination across quality processes (e.g., batch disposition, deviation management, change control, and release activities).

Implement best practices, digital solutions, and innovative approaches that enhance performance, scalability, and employee experience, while sharing learnings across the UCB quality network.

Ensure robust governance and periodic review of process performance, translating insights into targeted improvement plans with clear accountability and measurable outcomes.

Enterprise Leadership & Strategic Partnerships

Influence site and network strategy by bringing Quality, patient, regulatory and risk perspectives into key business decisions.

Partner with Manufacturing, Supply, Technical Operations, MSAT, Regulatory, Engineering and HSE leadership to deliver sustainable business and patient outcomes.

Build trusted relationships across the UCB network and use influence beyond formal reporting lines to accelerate decisions, resolve complexity and drive shared accountability.

Decision-Making Authority (Independence of the Quality Unit)

Authority to approve or reject materials, intermediates, DS and DP batches, and to refuse QP certification.

Authority to stop or suspend manufacturing, quarantine product or facilities where product quality or patient safety may be compromised.

Interested? For this position you’ll need the following education, experience and skills

Master’s degree or an education in a relevant scientific discipline

Significant experience in the pharmaceutical industry.

Fluent in French and English, on-site presence required.

Extensive senior-level Quality leadership experience, including experience leading other leaders.

Knowledge of worldwide GMP regulations and best practice, with special emphasis on injectables and aseptic manufacturing.

Act as a visible champion of Quality Culture and Operational Excellence, leading by example and fostering an environment of accountability, continuous improvement, and patient-focused decision-making across the organization

Proven track record across the biologics & pharmaceutical value chain, encompassing Drug Substance and Drug Product operations as well as critical enabling functions including validation, maintenance, and computerized systems

Extensive experience serving as the lead Quality representative during regulatory inspections, interacting directly with global health authorities including, but not limited to FDA and EMA.

Drive digital transformation and AI adoption by using data, technology, and automation to strengthen decision-making, boost productivity, and deliver business value.

Fact-based, risk-based decision making; accountability and delivery attitude.

Ability to collaborate and influence across departments and levels; excellent communication; team player and customer oriented.

Proven ability to manage complex budgets, build compelling resource and investment cases, and drive sustainable cost and efficiency improvements while maintaining operational effectiveness.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us 

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us? 

At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.