Director

• Maintain deep expertise in evolving methodologies, including proactive awareness of regulatory, Payer/HTA, and guideline/formulary evidentiary requirements.
• Review, synthesize, and disseminate external case studies and precedents to shape internal strategy and analyses.
• Act as key reviewer for the Global RWE Methods Review Board, ensuring robust governance and methodological consistency across programs.
• Lead the design of advanced study designs and statistical analyses aligned with Payer/HTA expectations (e.g., indirect treatment comparisons, causal inference methods, surrogate endpoint validations, etc.) to support market access and launch strategies for key assets.
• Provide key contributions to capability building, including training for team on Payer/HTA requirements and new methodologies and also in the development of coding libraries and AI/ML advanced analytics scaling and platforms, etc.

Director HTA Statistics – RWE Methods

• Provide strategic direction for the Johnson & Johnson Innovative Medicine Combination Product & Device Development initiatives
• Drive innovative thinking along with a disciplined approach for development, transfer and lifecycle management of new drug device combination products
• Take ownership of achieving and maintaining a robust compliance profile for Drug Device Combination Products
• Provide functional management to a team of Quality Engineers supporting new product development
• Act as a Combination Product & Device Quality Subject Matter Expert
• Oversee the revision of site / functional procedures related to Combination Product Development Process & Design Control

Director, Combination Product & Device PQM

• Provide strategic direction for the Johnson & Johnson Innovative Medicine Combination Product & Device Development initiatives while ensuring design control procedures are harmonized, integrated, understood & executed by key business partners across multiple departments and sites.
• Drive innovative thinking along with a disciplined approach for the rapid, compliant, high-quality development, transfer and lifecycle management of new drug device combination products across multiple sites while ensuring business and regulatory requirements are achieved.
• Take ownership of achieving and maintaining a robust compliance profile for Drug Device Combination Products across the JJIM development and supply chain sites. This includes proactive identification of risks, driving mitigation/remediation activities and supporting inspection readiness activities.
• Provide functional management to a team of Quality Engineers supporting new product development and lifecycle management of drug-device combination products.
• Act as a Combination Product & Device Quality Subject Matter Expert in global Health Authority inspections.
• Oversee the revision of site / functional procedures related to Combination Product Development Process & Design Control and provide training programs in the area of Combination Products.
• Act as a Qualified Trainer for the deployment of these and any other applicable training programs.
• Develop and apply advanced knowledge of advanced quantitative analysis, statistics, DoE etc.
• Support asset evaluation for licensing and acquisitions activity.
• Carry out duties in compliance with all local, state, and federal and international regulations and guidelines including FDA, EMA, EPA, OSHA, and global health authorities as applicable.

• Collaborate with the Functional template owners and Functional CoE, and lead the Governance process with respect to capability improvements
• In partnership with Technology, sustain and manage the content & configuration elements of the system solution including process flows
• Partner with Master Data and ensure Delivery of connected master data and transaction data excellence that support IM Operations
• Ensure compliance with the IM and Transcend processes
• Forge effective partnerships with IT, in the development of the connection points with the Integration layer and seamlessly connect to the enterprise architecture, visualization and analytics design
• Work closely with the other Strategic Programs Lead to continuously embed best practice and agile methodologies in the support of IM Transcend system
• Ensure support across functions is established and maintained for deployed capabilities
• Leverage best practices across the enterprise, drive preventative action, enable enterprise/E2E knowledge-sharing and act as an escalation point for critical user issues
• Develop sustainment infrastructure to oversee and assist Super Users in providing access and security controls support for the systems according to the defined processes
• Establish a team of experts to provide system audit and inspection support
• Ensure all support documentation aligns with the IM Quality Management System requirements, including creation, revision, review, and approval when it is required
• Ensure Sustainment functional teams understand the impact systems standards and architecture changes will have on the template capabilities and the need to engage with the Change Control Board
• Create and maintain infrastructure of Change Control Boards
• Facilitate Business Case justification for Continuous Improvement changes, and lead implementations ensuring business readiness through oversight of Business Adoption and Documentation/Training
• Partner with J&J Technology (JJT)
• Consistently seek to establish best practices in Functional CoE engagement through actively participating in Continuous Improvement opportunities
• Develop team resources that can achieve functional excellence and have the ability to become SMEs for multiple functional areas over time through participating in targeted development programs
• Partner with Transcend and IM colleagues
• Collaborate with senior leaders to ensure design aligns strategies and roadmaps
• Partner with global template team of Supply Chain experts in design, development, maintenance and improvement of global business processes and integration points

Director, GTO Innovative Medicine Operations

• Collaborate with the Functional template owners and Functional CoE, and lead the Governance process with respect to capability improvements
• In partnership with Technology, sustain and manage the content & configuration elements of the system solution including process flows
• Partner with Master Data and ensure Delivery of connected master data and transaction data excellence that support IM Operations
• Ensure compliance with the IM and Transcend processes
• Forge effective partnerships with IT, in the development of the connection points with the Integration layer and seamlessly connect to the enterprise architecture, visualization and analytics design
• Work closely with the other Strategic Programs Lead to continuously embed best practice and agile methodologies in the support of IM Transcend system
• Ensure support across functions is established and maintained for deployed capabilities
• Leverage best practices across the enterprise, drive preventative action, enable enterprise/E2E knowledge-sharing and act as an escalation point for critical user issues
• Develop sustainment infrastructure to oversee and assist Super Users in providing access and security controls support for the systems according to the defined processes
• Establish a team of experts to provide system audit and inspection support
• Ensure all support documentation aligns with the IM Quality Management System requirements, including creation, revision, review, and approval when it is required
• Ensure Sustainment functional teams understand the impact systems standards and architecture changes will have on the template capabilities and the need to engage with the Change Control Board
• Create and maintain infrastructure of Change Control Boards
• Facilitate Business Case justification for Continuous Improvement changes, and lead implementations ensuring business readiness through oversight of Business Adoption and Documentation/Training
• Partner with J&J Technology (JJT)
• Consistently seek to establish best practices in Functional CoE engagement through actively participating in Continuous Improvement opportunities
• Develop team resources that can achieve functional excellence and have the ability to become SMEs for multiple functional areas over time through participating in targeted development programs
• Partner with Transcend and IM colleagues
• Collaborate with senior leaders to ensure design aligns strategies and roadmaps
• Partner with global template team of Supply Chain experts in design, development, maintenance and improvement of global business processes and integration points.

Director, Innovative Medicine Operations

• Plan, design and execute multiple studies for a given asset and manage timelines, deliverables, and budget
• Assure quality of deliverables, including review and sign off project specifications, protocols, data analysis plans, final study reports, abstracts, posters and manuscripts, adherence to SOPs.
• Identify resources, references and analyses to inform scientific design and advise internal experts (clinical, commercial/market access) and external experts as needed in support of the asset team.
• Translate identified needs for evidence into study concepts in alignment with strategic objectives and vision for the asset, e.g. development of study protocols and proposing innovative and cost-effective ways of developing and executing studies
• Develop and maintain a good working knowledge of real-world data resources, existing partnerships and public initiatives and become the point person for select sources to advise on their suitability to address given research questions.
• Develop a deep understanding of customers’ needs, including HTA requirements, as well as the acceptance of RWE or economic evidence and impact to the decision making of different customers (reimbursement, medical societies, physicians).
• Collaborate with internal teams and participate in best practice sharing sessions across NIS organization.
• Build strong working relationships with stakeholder groups across medical, market access, R&D and commercial to ensure strategic alignment and optimal cross-functional collaboration and communication.
• Ensure key stakeholders including TA aligned business leaders are regularly updated on plans through periodic reporting.
• Develop excellent working relations with external thought leaders to ensure appropriate methods and research agendas are applied, in accordance with GSK policies.

Real World Evidence and Health Outcomes Director

• Smappee stands for Smart Appliance for Energy Efficiency. At the core of everything we do, we aim to facilitate energy efficiency in an innovative, easy, and fun way. Our cutting-edge technology empowers businesses and individuals to take control of their energy consumption, reduce costs, and contribute to a sustainable future. We're on a mission to make energy management smarter, more efficient, and environmentally friendly. Our offering focuses on energy management solutions and electric vehicle charging. With a global reach and a dynamic, rapidly expanding team, we're driving innovation and sustainability to power a brighter future.
• Smappee is looking for a results-driven Project Director to lead our Project Management Office and enterprise project portfolio. Combining strategic oversight with hands-on leadership, you will ensure the right projects are delivered in the right way, while continuously improving execution, governance and organizational effectiveness.
• **Responsibilities **Portfolio strategy & governance
• - Own and continuously optimize Smappee's enterprise project portfolio, ensuring initiatives are strategically aligned with business priorities and available execution capacity.
• - Partner with the senior leadership to evaluate, prioritize, sequence and challenge new initiatives based on business value, dependencies, risks, resources and financial impact.
• - Establish and maintain portfolio governance, providing clear visibility into project status, capacity, risks, budgets and delivery performance.
• Strategic project leadership
• - Personally lead the company's most business-critical, cross-functional and high-impact strategic initiatives.
• - Ensure projects are delivered on time, within scope and budget, while balancing quality, customer impact and organizational priorities.
• - Drive alignment across R&D, Product Management, Operations, Sales, Marketing and other business functions.
• PMO excellence
• - Build and continuously improve project management methodologies, governance frameworks, tools and reporting standards.
• - Challenge existing ways of working and drive continuous improvements to increase organizational effectiveness, speed and scalability.
• - Define and monitor portfolio KPIs to support data-driven decision making and continuous improvement.
• Leadership
• - Lead and coach the (small) Project Management team, fostering a culture of ownership, accountability and continuous development.
• - Provide direction, support and mentoring to Project Managers while directly managing selected strategic programs.
• - Promote collaboration across departments and create strong stakeholder engagement throughout the organization.

Project Director

• You will be responsible for leading and guiding the Oncology discovery research in selected cancer indications.
• The Executive Director, Discovery Oncology defines and executes on the strategy for Oncology Discovery.
• Develop a portfolio of therapeutics addressing core pathways in Oncology from project concept through to entrance into clinical trials.
• Leads a global group of approximately 20-40 people (including regular FTEs, temporary contractors and postdoctoral fellows), guiding their science with an emphasis on scientific quality and rigor.
• In partnership with Oncology leadership, including TA head, clinical, strategic and functional leaders, defines the scientific strategy for the TA and develops a portfolio of assets for solid cancer indications.
• Creates an environment that values innovation, leadership, scientific excellence, urgency, and personal accountability.
• Manages resource allocations across programs, included shared resources across labs.
• Proactively influences across functional areas and external partners to align project activities with strategic goals.
• Establishes internal and external collaborations to facilitate execution of Discovery strategy.
• Partners with external collaborators and innovation centers to evaluate and discover new approaches, technologies, and targets in support of the Oncology portfolio.
• Provides management oversight including personal talent development, training, coaching and guidance to discovery scientists.

Executive Director – Discovery Oncology

• Develop and execute the company’s policy evidence strategy for priority international policy issues.
• Serve as an external policy subject matter expert for the company on international policy research and economic issues.
• Oversee an array of research projects including economic modeling, HTA and evidence impact assessments, fiscal impact assessments, and relevant quantitative and qualitative data analyses as required.
• Develop economic policy research materials, white papers, publications and policy narratives that support BMS’s policy strategies.
• Proactively shape the policy and regulatory environment through dissemination & communication of policy research in external forums.
• Cultivate and manage external relationships with research institutions, consultants, and policymakers.
• Provide expert guidance to senior leaders to ensure policy evidence informs enterprise decisions.
• Drive cross-functional alignment on dissemination and messaging of policy research.
• Ensure analytical rigor and strategic relevance of all research & evidence generation.

Director, International Policy Research – Economics

• Drive AFME’s MIFID/MiFIR related advocacy work: partner with members and policy teams to establish clear advocacy objectives for our work in this strategic area for the organisation, in both the EU & UK. Formulate and deliver tailored positions, supporting analysis and tailored outreach plans with respect to relevant official sector stakeholders and private sector partners.
• Develop and execute advocacy plans in other policy areas depending on the evolution of the financial services policy landscape and the organisation’s priorities
• Working closely with our communications team, drive public communication strategies across key regulatory issues.
• Actively shape AFME’s strategic advocacy priorities and contribute to AFME-wide initiatives to relay these to senior official sector stakeholders; provide high-level briefings to senior management and relevant member committees as needed.
• Leverage and grow a network of contacts including relationships within the European Commission, the European Parliament, ESMA, Member States, NCAs and UK authorities.
• Build industry collations with trade associations representing the financial service industry and beyond, including the buy-side, financial market infrastructures, corporates and civil society, understanding their positions and objectives.
• Represent the association’s views in various associations, fora, at conferences, etc.
• Contribute to our international engagement as part of GFMA, AFME’s global umbrella organisation.

Director, Advocacy

• Lead initiatives to improve portfolio planning system processes, ensuring alignment with organizational goals.
• Support the development of portfolio data quality metrics to foster continuous improvement.
• Lead data quality efforts, identifying gaps, and prioritizing data management initiatives.
• Partner with business teams to implement process improvements and technology solutions that elevate operational data integrity.
• Apply data quality metrics to track progress and support informed decision-making.
• Act as a Project Manager to increase transparency of planning initiatives, leading timelines, resources, and risks.
• Drive standardization of planning activity definitions across Johnson & Johnson Innovative Medicine (JJ IM) Therapeutic Areas (TAs) and Global Development partners.
• Collaborate with PPR teams to develop and refine planning insights for senior leadership.
• Support the Business Product Owner of Planisware (E7) and the User Community Tool (UCT) Planning products. This includes making recommendations on new capabilities and/or improvement to current systems, coordinating the UAT, training and adoption in partnership with Portfolio Solutions and IT.
• Reinforce planning data quality via metrics, communication, and process reinforcement to the Planning community to maintain a high degree of portfolio project data integrity.
• Provide leadership and support to the Business Product Owner of the User Community Tool (UCT) and Planisware (E7), leading UAT, training and adoption of new processes associated with tool enhancements to end users.

Associate Director, Planning System Lead

• You define and oversee all analytical development and GMP-compliant QC activities across small and large molecule projects, ensuring scientifically sound and phase-appropriate approaches.
• You plan and organize departmental activities and resources to consistently meet or exceed targets related to quality, productivity, timelines, and capacity.
• You drive the implementation of new analytical techniques, technologies, and digital solutions, in close collaboration with validation and maintenance, to expand the service offering and improve efficiency.
• You lead, coach, and develop Group Leaders and (Associate) Scientists, ensuring clear goal setting, strong performance management and continuous team development.
• You support the professional growth of team members through structured feedback, coaching, and targeted training initiatives.
• You collaborate closely with cross-functional stakeholders (Formulation Development, Production, Quality, Project Management) to resolve issues, define priorities, and translate these into clear, actionable plans.
• You provide strategic and technical input to client proposals, defining appropriate analytical strategies aligned with project scope and regulatory expectations.
• You are a member of and contribute to the local Management Team, actively supporting site strategy, operational decisions, and continuous improvement initiatives.
• You demonstrate the ability to strategically leverage AI and digital technologies to enhance Analytical Development performance, decision‑making, and innovation. You apply AI in a compliant, data‑driven manner to improve efficiency, quality and scientific insight, while guiding your team in responsible and effective AI adoption.
• You report to the Site Head of the Drug Development & Manufacturing Business Unit.

Director Analytical Development

• Provides advanced scientific expertise in the safety evaluation and risk management of key GSK oncology assets in clinical development.
• Leads the identification, assessment, and communication of safety risks to ensure robust benefit-risk profiles and protection of patients globally.
• Drives the evaluation and interpretation of safety data, including signal detection and assessment.
• Develops strategic approaches for safety issue evaluation within clinical development programmes.
• Contributes to safety components of global regulatory submissions (e.g., INDs, DSURs, IBs).
• Ensures high-quality, timely delivery while managing multiple priorities.
• Represents Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project Teams.
• Leads cross-functional efforts to address urgent and complex product safety issues.
• Partners closely with Safety Physicians and stakeholders to prepare for and contribute to Safety Review Team (SRT) meetings.
• Escalates emerging safety issues to senior leadership and governance bodies as appropriate.
• Communicates complex scientific information clearly to a range of audiences.

Scientific Director, SERM

• Central point of contact for all Quality-related matters within the organization
• Developing and implementing quality policies and procedures
• Leading the Quality department and ensuring necessary training and development of employees
• Supervising and participating in internal and external audits
• Analyzing quality data and reporting findings to the Management Team
• Collaborating with GMP Production, R&D, and analytical department to resolve quality issues
• Shaping strategy and processes for the Ghent site within the Ardena group
• Reconciling business objectives with legal quality requirements
• Ensuring AI is effectively embedded across quality processes

Quality Director

• You are the strategic and operational leader responsible for defining and executing Carrefour Belgium's credit and collection strategy.
• You build sustainable and financially sound partnerships with franchise partners, suppliers and customers.
• You drive operational excellence across the entire Order-to-Cash process.
• You define and optimize the financial strategy, credit policy and collection approach towards franchisees, suppliers and various customers.
• You determine credit limits and methods to cover financial risks (such as guarantees and credit insurance).
• You systematically support franchise partners on financial parameters at every stage of the collaboration.
• You are ultimately responsible for the timely, accurate and legally compliant issuance and processing of all outgoing invoices.
• You continuously optimize the end-to-end (E2E) invoicing process.
• You implement the factoring agreement with the bank and prepare finance committees together with Regional and Zone Directors.
• You lead, motivate and develop a team of 15 professionals in line with Carrefour's leadership model.

Director jobs in Belgium

See all jobs on JobTailor

Director HTA Statistics – RWE Methods

Director, Combination Product & Device PQM

Director, Combination Product & Device PQM

Director, GTO Innovative Medicine Operations

Director, Innovative Medicine Operations

Real World Evidence and Health Outcomes Director

Project Director

Executive Director – Discovery Oncology

Director, International Policy Research – Economics

Director, Advocacy

Associate Director, Planning System Lead

Director Analytical Development

Scientific Director, SERM

Quality Director

O2C Credit Management Director