AM Engineering Projects

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

• Lead integration of Cognex (or equivalent) vision systems for inspection, verification, and traceability.

• Define vision system requirements, acceptance criteria, and commissioning strategy.

• Support long‑term system reliability and performance.

• Review and approve electrical schematics, panel layouts, loop diagrams, and instrumentation selection.

• Ensure compliance with electrical codes, functional safety, and regulatory standards.

• Coordinate electrical installation, testing, and commissioning activities.

• Ensure projects comply with EHS, machine safety, GMP, Quality Systems, and Data Integrity requirements.

• Lead or support IQ / OQ / PQ execution for automated equipment.

• Own deviations, root cause investigations, and CAPA implementation related to automation or equipment.

• Maintain audit‑ready project and validation documentation.

• Coordinate with Manufacturing, Quality, Validation, IT/OT, Supply Chain, Procurement, and Global Engineering teams.

• Provide technical mentoring and task leadership to junior engineers or automation resources.

• Communicate project progress, risks, and mitigation plans to engineering leadership.

Demonstrated working knowledge and practical application of:

• Experience in regulated manufacturing (MedTech / Pharma) preferred.

• Ability to find root cause through QMS driven approach & awareness of CAPA Process