The Senior Capital Projects Manager leads major capital investment projects (€20M+) and drives the development and continuous improvement of HAL's Project Management Office (PMO). The position combines project leadership, governance, and portfolio oversight to ensure successful delivery of strategic projects and sustainable project management practices across the organization. The Senior Capital Projects Manager works closely with Manufacturing, Engineering, Quality, Regulatory Affairs, R&D, Supply Chain, Finance, and external partners to deliver business objectives and strengthen project management capabilities across HAL.

Relocation support may be available for exceptional international candidates.

Project leadership

• Lead end-to-end delivery of major capital investment projects (€20M+) from business case development through execution, commissioning, operational handover, and lifecycle management.
• Develop and maintain integrated project plans, schedules, budgets, resource forecasts, and risk to deliver agreed scope, quality, timeline, and cost objectives.
• Lead cross-functional teams and manage project dependencies, risks, issues, and escalations to achieve key business and project milestones.
• Drive project governance, performance monitoring, and KPI-based reporting, providing clear and timely updates to SteerCo, senior leadership, and key stakeholders.
• Deliver complex manufacturing, facility, and infrastructure projects that support HAL's strategic objectives.

PMO & Governance

• Establish, maintain, and continuously improve HAL's PMO, including governance, project standards, tools, and reporting.
• Drive portfolio management, project prioritization, resource planning, and executive decision-making processes.
• Develop KPI dashboards and portfolio reports and facilitate governance and project review meetings.
• Train and mentor HAL employees, standardize project management practices, and promote PMO best practices across the organization.

Stakeholder Management

• Build and manage strong relationships with senior leaders, cross-functional teams, suppliers, contractors, and other key stakeholders.
• Lead cross-functional project teams including Manufacturing, Engineering, Quality, Supply Chain, Technical Services, Validation, Regulatory Affairs, and Finance.
• Align project execution with business objectives and serve as a trusted advisor to project teams and stakeholders.
• Facilitate SteerCo and governance meetings to support effective project oversight and executive decision-making.
• Communicate project status, progress, risks, mitigation plans, and recommendations clearly to all levels of the organization.
• Manage external partners, including equipment suppliers, engineering firms & consultants.

Risk & Compliance Management

• Identify, assess, and manage project risks and opportunities, ensuring effective mitigation and escalation where required.
• Oversee project budgets, forecasts, and financial performance.
• Conduct scenario planning and portfolio impact assessments.
• Ensure effective change control and scope management practices.
• Ensure all projects comply with GMP, EHS, quality, validation, and regulatory requirements.
• Ensure successful completion of FAT, SAT, Commissioning, Qualification, and Operational Readiness activities.

Continuous improvement

• Lead initiatives to improve project delivery capabilities and organizational maturity.
• Implement lessons learned and best practices across the portfolio.
• Support digital transformation and implementation of PMO tools and reporting solutions.
• Mentor and coach project managers and project team members.

• Bachelor’s or master’s degree in engineering, Pharmaceutical Sciences, Biotechnology, Manufacturing, or related discipline.
• 10+ years of project management experience in pharmaceutical, biotech, medical device, or other highly regulated environments; Six Sigma Black Belt certification is highly preferred.
• Proven track record delivering complex capital projects (€20M+) and leading cross-functional programs.
• Experience establishing and developing PMO capabilities, including portfolio governance and project prioritization.
• Strong knowledge of GMP-regulated environments and pharmaceutical development, manufacturing, and commercialization processes, including Computer System Validation (CSV), Annex 1 requirements, and sterile injectable manufacturing processes.
• Demonstrated ability to drive quality and compliance initiatives in pharmaceutical operations; experience with TrackWise and other quality management platforms is considered a strong advantage.
• Experience managing senior stakeholders, governance committees, engineering partners, OEMs, EPCM firms, and contractors.
• Proficient in project and portfolio management tools (e.g., MS Project, Smartsheet); PMP/Prince 2 certification required.
• Fluent in English; Dutch is an advantage.

You are a hands-on project leader who combines technical knowledge, quality awareness and strong stakeholder management skills. You thrive in complex regulated environments and are comfortable leading multidisciplinary teams through challenging CAPEX projects while maintaining compliance, quality and business focus.

We look forward to hearing from you! We are interested in your CV, but we also want to find out more about your ambitions, your personality and what drives you to apply. So be sure to include a brief cover letter telling us why you are a match for this position. The application process consists of an introduction by the Recruiter, three interviews either via video call or live at our office in Leiden with the Hiring Manager and/or a Department Specialist and the CEO followed by contract negotiations. Depending on the vacancy, an assessment could be part of the process.

HAL Allergy does not accept unsolicited approaches from recruitment agencies and/or search firms (such as, for instance, the sending of resumes) for any job posted on this or a referring website. All recruitment agencies and search firms are required to contact HAL Allergy Recruitment via recruitment@hal-allergy.com to enquire about a potential recruitment or search agreement with HAL Allergy.

HAL Allergy is one of the European top players in the development, production and distribution of allergen immunotherapies for the treatment and prevention of allergic diseases. We focus on the development and manufacturing of modified allergen extracts for the therapeutic and diagnostic purposes of respiratory and food allergies. With all our activities the patient's well-being is always top of mind. At Hall Allergy we foster open discussions, an entrepreneurial spirit and close collaborations within the teams and with our international colleagues summing up to more than 300 highly specialized people across various positions. If you too would like to become a part of an innovative and challenging pharmaceutical manufacturer, then this is your perfect opportunity!

HAL Allergy is headquartered in Leiden, where all disciplines work under one roof, from development to sales. We work in an informal, culturally diverse organization with room for growth and continued personal development. HAL Allergy is located in the middle of the thriving and energetic Leiden Bio Science Park, the largest innovation district of the Netherlands in the field of Life Sciences & Health. The central train station and the ancient city center of Leiden are just a 5 minute bike ride away from our office.