Senior Program Manager
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Location:
Zaventem, Belgium
Experience:
10 years We are seeking an experienced Senior Program Manager to support and drive complex global pharmaceutical manufacturing programs. The successful candidate will bring strong program management expertise along with domain experience in regulated pharmaceutical environments. Mandatory Requirement: Experience in at least one of the following areas is essential:
• Cleaning Validation
• Nitrosamine Risk Assessment and Remediation Programs
• Biologics Manufacturing
Key Responsibilities
• Lead and coordinate complex global programs involving multiple workstreams, stakeholders, and manufacturing sites.
• Develop and maintain integrated project plans, milestones, dependencies, critical paths, and governance frameworks.
• Drive alignment across Manufacturing, MSAT, Quality, Regulatory, Compliance, Supply Chain, and Technical Operations teams.
• Manage program risks, issues, decisions, actions, and mitigation plans.
• Prepare and present executive-level status reports, dashboards, and governance materials.
• Ensure effective communication between global functions and site teams.
• Support implementation, deployment, training, and change management activities.
• Identify barriers to execution and drive resolution to maintain program delivery timelines. Required Experience
• Significant Program or Project Management experience within Pharmaceutical, Biotechnology, Life Sciences, Manufacturing, Quality, MSAT, Technical Operations, or Supply Chain environments.
• Proven success managing large-scale global programs with multiple concurrent workstreams.
• Strong understanding of GMP-regulated environments.
• Experience with program governance, integrated planning, risk management, dependency tracking, and stakeholder engagement.
• Ability to manage and influence cross-functional teams within a global matrix organization.
• Excellent leadership, communication, and stakeholder management skills. Preferred Experience
• Cleaning Validation lifecycle management.
• Nitrosamine risk assessment, compliance, and remediation programs.
• Biologics manufacturing and operations.
• Contamination control and cross-contamination risk management.
• Drug Substance and Drug Product manufacturing.
• Global deployment of quality, regulatory, or technical standards.
• Microsoft Project and enterprise project portfolio management tools. Ideal Candidate The ideal candidate will be capable of translating complex technical and regulatory requirements into structured execution plans while maintaining visibility across program deliverables, risks, dependencies, timelines, and stakeholder expectations. About HCLTech HCLTech is a leading global technology company, empowering enterprises with innovative digital, cloud, engineering, and cybersecurity solutions. With a strong presence in the Netherlands since 1999, HCLTech partners with organizations to accelerate transformation, drive operational excellence, and deliver business value. Join our diverse and collaborative team in The Hague and help build next-generation technology solutions for global clients.
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