Global Automation Standards Lead

Johnson & Johnson

Lead global Automation Standards & Governance for Johnson & Johnson's manufacturing sites. Ensure compliance and promote standardization across Process Automation Systems in biopharmaceutical manufacturing.

Posted 7/10/2026full-timeAthens • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Automation Standards and Process Automation Systems (PAS) within a GMP-regulated manufacturing environment, with a strong focus on continuous improvement and stakeholder management.

Highest-signal resume keywords

Automation Standards DevelopmentIndustrial Automation SystemsGMP-Regulated ManufacturingISA S95 and S88 StandardsStakeholder Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Process Automation SystemsPLCSCADADCSMES IntegrationAutomation Global LibrariesRecipe ManagementProcess ControlData HistorianComputer System Validation

Soft Skills

Communication SkillsCross-Functional Team Leadership

Industry Keywords

Biopharmaceutical IndustryPharmaceutical IndustryCGMP RegulationsContinuous ImprovementManufacturing Environment

About the role

Key responsibilities & impact

Develop, own, implement, and govern the Automation Standards across all Process Automation System (PAS) platforms
Ensure robust, fit-for-purpose design standards and promote standardization where it adds value
Champion the implementation of these Standards across the manufacturing network
Continuously monitor adherence to the standards and identify opportunities for improvement
Own and manage Automation global libraries, recipe management, process control, and data historian activities
Develop and maintain a road map of current and future Process Automation Systems (PAS)
Support continuous improvement in identifying potential improvements across all Process Automation System platforms

Requirements

What you’ll need

BS. Degree in Engineering, Science or related discipline
Minimum of 12 years of experience in a manufacturing environment, preferably within the biopharmaceutical or pharmaceutical industry
At least 10 years of proven experience in an Automation, OT or IT role within a pharmaceutical or GMP-regulated manufacturing environment
Proven track record in leading cross-functional teams and driving global initiatives in automation and process control
Deep understanding of industrial automation systems, including PLCs, SCADA, DCS, and integration with MES and IT systems
Expertise in ISA S95 and S88 standards
Knowledge of cGMP regulations related to Automation & Computer System Validation (CSV)
Strong stakeholder management and communication skills

Benefits

Comp & perks

Inclusive work environment
Professional growth opportunities
Strong emphasis on diversity and merit