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 https: //www.jnj.com

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JOB SUMMARY

Established and productive individual contributor in a scientific/technology field. Administers automation for modernized and legacy systems, infrastructure, and services. Conducts the planning, design, scheduling and control of Manufacturing Systems projects and process improvements. Contributes to key performance indicator achievements and supports company initiatives.

DUTIES & RESPONSIBILITIES

• Installs equipment and control systems and helps determine reliability and need for updates.
• Documents automation project requirements in support o project management, process improvements and maintenance.
• Conducts routine assessments to determine regulatory compliance and any necessary improvements for regulation conformity.
• Completes automation deliverables and ensures adherence to expected deadlines.
• Analyzes complex changes in scope, including provision of necessary information to support claims for time and cost impact.
• Communicates with subject matter experts regarding workflow and project deliverables internally and externally.
• Coaches more junior colleagues in techniques, processes, and responsibilities.
• Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed

EXPERIENCE AND EDUCATION

ESSENTIAL:

• 2 years industry experience in life science or related industry
• Education Requirements: Hons Degree in Engineering, Science or a related discipline
• PLC Programming
• Experience in delivery of automation projects
• Ability to interpret engineering drawings/specifications
• Working knowledge of Medical Device Quality Systems within a regulated environment

DESIRABLE:

• Experience in computer system validation.
• Experience with manufacturing systems
• Experience with Database Configuration and Maintenance
• Experience with IT Networks

REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS

• High attention to detail
• Pro-active approach to work
• High standards
• Flexible
• Excellent Communication and presentation skills
• Analytical skills
• Team Player
• Highly computer literate
• Planner & Organiser
• Project Management
• Active Listener
• Continuous Improvement focus