OneLIMS Program Lead

Sanofi; Barcelona; Presencial; EUR 120.000 - 180.000; Jornada completa

Descripción de la vacante

Sanofi is seeking a senior program leader to orchestrate the OneLIMS initiative, modernizing LIMS across the global QC lab network. You will drive strategy, governance, and cross-functional collaboration with stakeholders from Quality, Manufacturing, and IT.

Responsibility spans budget, ROI, and ensuring GxP compliance across sites. Applicants bring 10+ years in pharma project leadership, deep experience with LIMS or quality systems, and a track record of delivering large-scale digital

Formación

• 10+ years of program/project management in pharma/biotech/life sciences
• 5+ years in senior program leadership roles
• Experience managing multi-site, global programs with significant budget responsibility (>€10M)
• Hands-on with LIMS or enterprise quality systems
• Deep understanding of GxP, regulatory requirements (FDA, EMA)

Responsabilidades

• Define and drive OneLIMS program strategy, roadmap, and business case with stakeholders
• Chair governance across Quality, GBUs, Manufacturing Operations
• Frame program structure including governance, budget, and communication
• Lead multi-site LIMS deployment ensuring on-time, on-budget delivery
• Manage budgets (OPEX/CAPEX) and ROI tracking
• Ensure compliance with GxP, data integrity, and cybersecurity
• Coordinate interdependencies across workstreams and report progress to leadership

Conocimientos

Portfolio management

Stakeholder management

Change management

Digital transformation

Risk management

Program leadership

Budget oversight

Educación

Master's degree in Life Sciences, Computer Science, Engineering, Business Admin

PgMP preferred; PMP minimum

Herramientas

MS Project

JIRA

Confluence

Descripción del empleo

About The Role

The

• Location: Barcelona, Spain

About The Role

The OneLIMS program is a strategic global initiative to modernize and standardize Laboratory Information Management Systems (LIMS) across Sanofi's entire worldwide QC laboratory network.

The program aims at delivering a unified, compliant, and future-ready digital platform and carries significant impact, touching hundreds of users across Sanofi's global operations.

At Sanofi, we are an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system — and innovative pipeline — enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

Main Responsibilities

Strategic Leadership & Governance

• Define & drive the OneLIMS program strategy, roadmap, and business case, jointly with our business stakeholders, ensuring alignment with Sanofi's digital transformation and quality excellence objectives
• Chair program governance across Quality, GBUs, Manufacturing Operations, ensuring rigorous decision‑making and executive-level visibility
• Frame the program structure in terms of Project Leaders, governance bodies, communication strategy, and budget architecture
• Ensure alignment and manage interdependencies with other strategic programs (ERP program, QC Lab instruments connectivity and other initiatives), coordinating with parallel workstreams to avoid conflicts, maximize synergies, and maintain visibility on cross-program impacts

Program Delivery & Value Realization

• Lead complex, multi-site LIMS implementation and deployment across Sanofi's global laboratory network, coordinating global and local teams to ensure on‑time, on‑budget, and compliant delivery
• Manage program budget (OPEX/CAPEX) and resource allocation with full financial accountability, including business case development and ongoing ROI tracking
• Measure and track benefits realization post-deployment — establish KPIs and metrics to quantify program gains, monitor ROI, and report on value delivered vs. business case commitments
• Guarantee consistency and compliance of program solutions, including GxP regulations, data integrity principles, and cybersecurity requirements
• Coordinate deliverables and interdependencies across workstreams, reporting Progress, risks, and achievements to senior leadership and governance bodies

Risk, Change & Stakeholder Management

• Manage cross‑functional stakeholder relationships at all organizational levels — from site teams to executive leadership — ensuring alignment, transparency, and shared accountability
• Foresee smooth system integrations, acting as primary point of contact for external partners and partnering systems
• Proactively identify, assess, and mitigate program risks, escalating critical blockers in a timely manner
• Ensure smooth user adoption, sustainable value realization, and continuous improvement across all impacted communities
• Foster innovation and leverage AI and emerging technologies to accelerate program efficiency and deployment

About You

Qualifications & Experience

• 10+ years of professional experience in program/project management within the pharmaceutical, biotechnology, or life sciences industry, including 5+ years in senior program leadership roles
• Proven track record managing complex, strategic, multi-site programs with global scope and significant budget responsibility (>€10M)
• Extensive hands‑on experience with Laboratory Information Management Systems or similar enterprise-level scientific or quality systems
• Deep background in GxP‑regulated environments, with solid understanding of quality, compliance, and regulatory requirements (FDA, EMA, data integrity)
• Demonstrated ability to lead organizational transformation and change management in complex, matrixed, multicultural environments

Required Skills

• Advanced portfolio management and project resource management capabilities
• Advanced business case development and financial management skills, including OPEX/CAPEX oversight and ROI analysis
• Advanced stakeholder management and vendor management expertise, with demonstrated ability to engage effectively at all levels — from site teams to executive leadership
• Advanced change management and business process re‑engineering (BPR) experience in large-scale digital transformation programs
• Strong understanding of QC laboratory operations, quality systems, and scientific workflows
• Deep knowledge of regulatory compliance frameworks (GxP, FDA, EMA, data integrity, cybersecurity)
• Proven ability to manage program budgets and allocate resources across complex, interdependent workstreams
• Advanced risk management and structured problem‑solving abilities
• Advanced Experience leading digital transformation initiatives in laboratory or manufacturing settings
• Cultural intelligence and ability to work effectively across diverse, global teams and geographies
• Innovation mindset with focus on leveraging emerging technologies to deliver competitive advantage

Technical Skills

• Advanced proficiency with program and project management tools (MS Project, JIRA, Confluence, or equivalent)
• Advanced data analysis and reporting capabilities to track program performance and communicate insights to senior leadership
• Strong understanding of system integration concepts and IT architecture in regulated environments
• Experience with business intelligence and analytics tools

Education

• Master's degree in Life Sciences, Computer Science, Engineering, Business Administration, or related field (required)
• Professional certification in program management (PgMP preferred; PMP minimum)
• Additional certifications in change management or digital transformation are advantageous

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