Experienced Automation Engineer, LCM MSAT

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

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About Innovative Medicine:

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at are searching for the best talent for an Experienced Automation Engineer LCM MSAT that will be based in Spring House PA or Raritan NJ.

An internal pre-identified candidate for consideration has been identified. However all applications will be considered.

Purpose:

TheExperienced Automation Engineer LCM MSATwill lead global initiatives to implement critical process closure projects that enhance reliability innovation and sustainability across our manufacturing sites. This role demands balancing diverse requirements across early development clinical trials and commercial production while collaborating effectively within a global network.

Key responsibilities include leading global initiatives supporting automated systems selection and integration process closure experience and driving these improvements through implementation. The ideal candidate will bring a strong background in automation engineering process closure technology equipment qualification and digital technologies with a passion for advancing innovation within a regulated environment.

Key Responsibilities:

Automation & Process Closure Integration

• Lead the design specification and deployment of automation systems for new and existing equipment across the CAR-T network from early concept to global implementation.

• Experience with process closure and containment technologies including isolators weldable solutions and other automated systems. Familiarity with data analyses and data leveraging which support the design implementation and validation of these technologies.

• Collaborate with cross-functional teams to ensure seamless automation and process closure technology integration into global site processes.

• Support procurement vendor engagement business case development and project costing analyses to support required business processes for implementation.

• Provide detailed data to support updates for project teams and high-level summaries for executive-level decision-making.

• Oversee equipment commissioning qualification (IQ/OQ/PQ) and lifecycle documentation in compliance with GMP CSV and Data Integrity standards.

• Partner with MSAT Quality IT and R&D teams to identify automation opportunities reduce variability and optimize network performance.

• Continuously analyze network performance and produce concepts which support COGM reduction robustness and efficiency.

• Develop KPIs and use them to monitor operational performance and identify improvement areas.

• Drive change management initiatives including communication plans and risk mitigation strategies (including FMEA development to support projects).

System Support & Troubleshooting

• Provide technical support for automation systems including PLCs SCADA MES and control platforms.

• Troubleshoot automation issues to minimize downtime and ensure operational continuity.

• Maintain thorough system documentation and quality records.

• Lead investigations and root cause analyses related to automation failures and process deviations.

Qualifications:

• Bachelors or Masters degree in Automation Engineering Electrical Mechanical Mechatronics or related fields.

• Minimum 4 years (2 years with a Masters degree) of proven experience in automation within GMP-regulated manufacturing.

• Deep knowledge of cGMP guidelines and regulatory standards (EMA FDA etc.).

• Strong understanding of process closure/containment technologies control systems and equipment integration.

• Self-directed detail-oriented with excellent critical thinking problem-solving project management and communication skills.

• Proven ability to manage projects and collaborate cross-functionally.

• Familiarity with drug development manufacturing processes and submission requirements.

• Proficiency in English (written and spoken).

• Willingness to travel up to 10% depending on project needs.

• Experience with PLC programming SCADA MES and data platforms.

• Familiarity with data historians digital twins and Industry 4.0 technologies.

• Knowledge of validation practices and regulatory requirements for automated systems.

• Exposure to digital transformation data analytics and cross-functional initiatives.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected vertebras and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is :

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