Site Automation Lead

Bij Johnson & Johnson geloven we dat gezondheid alles is. Onze kracht op het gebied van innovatie in de gezondheidszorg stelt ons in staat een wereld op te bouwen waar complexe ziekten worden voorkomen, behandeld en genezen, waar behandelingen slimmer en minder invasief zijn en oplossingen persoonlijk zijn. Dankzij onze expertise op het gebied van innovatieve geneeskunde en MedTech bevinden we ons in een unieke positie om vandaag de dag te innoveren in het volledige spectrum van zorgoplossingen om de doorbraken van morgen te realiseren en een grote impact te hebben op de gezondheid van de mensheid. Ga voor meer informatie naar jnj.com.

In navolging van ons Credo is Johnson & Johnson verantwoordelijk voor onze medewerkers die wereldwijd met ons samenwerken. We bieden een inclusieve werkomgeving waarin elke persoon als individu wordt beschouwd. Bij Johnson & Johnson respecteren we de diversiteit en de waardigheid van onze medewerkers en erkennen we hun verdiensten.

Functie:Supply Chain Engineering

Subfunctie functie functie:Automation Engineering

Functiecategorie:People Leader

Alle vacaturelocaties:Leiden, South Holland, Netherlands

Functieomschrijving:

Site Automation Lead

Johnson & Johnson is currently seeking a Site Automation Lead to join our Global Engineering & Technology organization located at the manufacturing site in Leiden, The Netherlands.
 

Position Summary:

You lead the site’s automation organization, owning the lifecycle of ISA‑95 Level 1–2 and selected Level 3 systems, ensuring compliance, reliability, and performance in a regulated environment. As part of the GET Leiden Leadership Team, you define and execute the automation strategy, translating business priorities into scalable, value‑driven solutions.
 

You drive automation delivery and system reliability while leading a high‑performing team and partnering across Operations, Quality, MSAT, Engineering, and IT/Digital to advance innovation, compliance, and operational excellence.
 

This role requires a strong people leader and change agent who can influence across a matrix and lead digital transformation.
 

What you will do

• Lead & Develop the Organization
  Lead and develop a high-performing automation organization (individual contributors, supervisors, managers), driving engagement, capability growth, succession planning and strong performance management.
• Define & Execute Automation Strategy
  Own and deploy the site automation and execution systems strategy, ensuring standardization, architectural alignment, and consistency across the platform.
• Drive Digital & Operational Excellence
  Advance the digital manufacturing roadmap and continuously improve automation systems by identifying upgrades, optimizing performance, and aligning with site and enterprise priorities.
• Deliver Automation Portfolio
  Lead automation and data-driven projects, ensuring compliant, safe, on-time, and within-budget delivery, including proper documentation and change control of all system modifications
• Ensure Compliance & Reliability
  Maintain GMP and EHS compliance, including SOP adherence, deviation/NCR investigation, CAPA management, and continuous audit readiness.
• Own Execution Systems & Lifecycle Management
  Oversee full lifecycle management of execution systems, including design (FS/DS), validation (FAT, SAT, IOPQ), system integration, interfaces, master data/recipes, and lifecycle documentation.
• Provide Technical & Operational Leadership
  Direct system performance, reliability, upgrades, and continuous improvement; ensure effective 24/7 system support, manage infrastructure (incl network in partnership with IT) and data system performance.
• Stakeholder & Vendor Management
  Partner cross-functionally (Operations, MSAT, Engineering, IT, DOTS) and manage vendors/contracts; provide input to capital projects, platform standards, and recipe/library development.
• Governance & Continuous Improvement
  Define policies and procedures, monitor KPIs, and drive continuous improvement using best practices, ensuring systems are fit for use and aligned with regulatory and business requirements.

Who you are:

• BSc degree in Engineering, Science or related technical field or a related field with 10+ years of experience in a manufacturing environment, biopharmaceutical OR an advanced degree MSc/MBA/Ph.D. or equivalent with 8+ years.
• 4+ years of leadership and delivery experience AND 4+ years of proven experience within a pharmaceutical or GMP regulated manufacturing environment in automation or IT role.

Role requirements:

• Proven ability to lead technical teams, manage competing priorities, and consistently deliver results in a complex, multi-stakeholder environment.

• Strong knowledge of cGMP in FDA-regulated environments, including validation practices (FAT, SAT, IO/PQ) and GAMP principles.
• Solid understanding of engineering documentation and compliance requirements for execution systems.

• Deep technical expertise in ISA-95 Level 1–3 systems (e.g., DeltaV, PLCs, MES PAS-X, OSI PI, infrastructure).
• Good understanding of Level 4 systems (ERP, Quality, Data platforms) and their integration.
• Strong grounding in ISA-95 and ISA-88 standards and their application in a global supply chain context.

• Demonstrated strategic thinking with experience in project and financial management.
• Ability to translate business needs into technical solutions and drive value realization.

• Strong stakeholder management skills with the ability to influence across a matrix organization and lead change.

• Fluent in English; Dutch is a plus.

#LI-MV2

 

 

Required Skills:

 

 

Preferred Skills: