Maintenance Supervisor

Description

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 Description:

Maintenance Supervisor

Are you ready to take on a unique and exciting opportunity as a Maintenance Supervisor in the Medical Device Sector? Johnson & Johnson is seeking a highly motivated individual to join our team in Nijmegen, Netherlands with an unlimited contract . This is your chance to be part of a world-class organization that is committed to innovation and delivering flawless quality in everything we do.

As the Maintenance supervisor, you will have the opportunity to lead a team of exceptional professionals and contribute to the success of our goals.

Under the direction of the Engineering Manager, Maintenance supervisor will provide technical leadership and expertise to drive continuous improvement in process and asset reliability through the detection and elimination of defects. In this role, the Maintenance supervisor will optimize the availability and productivity of our manufacturing facilities and equipment, perform engineering reviews, coordinate repair work, and participate in the commissioning and installation of new equipment.

This role also includes all people leader activities, support on project executions, challenging the team by technical solution and validations, standardize the way of working within the team and creation a good atmosphere within the team. In this job, the maintenance supervisor will use engineering principles, tools and techniques to develop, and optimize, and support systems and processes that are aligned with the overall Company strategy and mission.

Responsibilities:

Under the direction of the Engineering Manager and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Advanced courses on cGMP Internal:
• preferable: Process Excellence/Lean belt – Green Blet project leader, methodology, Risk Management - and Auditing experience – you have
• masters degree
• Analytical, innovative, and pragmatic thinking - YES
• maintenance problems associated with installation of manufacturing equipment and other utility equipment.
• Identify Continuous improvement opportunities within the Maintenance scope.
• Develop and Follow performance metrics (KPIs) and initiate appropriate actions.
• Lead technical investigations as required for specific projects/tasks.
• Partner with the process engineers to ensure the correct level of maintenance/servicing for all the processes.
• Manage Improvement projects in maintenance.
• Managing, coaching, and developing maintenance & calibration engineers/technicians through regular follow ups on uniform implementation of activities with the aim of good cooperation and efficiency of the maintenance organization.
• Develops department goals and objectives and conduct performance reviews to the team.
• Develops and implements preventive maintenance and instrument calibration programs and ensures programs are effective.
• Prepares and implements career development programs for direct reports.
• Follow compliance and EHS policies and guidelines.

Requirements:

• University / Bachelor’s Degree, Engineering degree or Equivalent in a Life Science,
• Process Engineering, or Physical Science. An advanced degree, such as Master degree in a Technical or Science field is preferred.
• Maintenance Experience with 4-8 years of leading technical departments preferably in GMP environment
• Experience in Maintenance, Calibration or Manufacturing and/or Engineering working on manufacturing processes and improvements.
• Strong written and oral communication in English required.
• Experience in the Medical Device industry and GMP.
• Demonstrated knowledge of manufacturing principles and practices, and procedures.
• Equipment and Process Validation / Establish Equipment requirements (URS, FAT, SAT)
• Capable to interpret the vendor maintenance/calibration/qualification reports to verify the effectiveness of the vendor’s work and adopt the outcomes into the process.
• Project management.
• Lean and/or Six Sigma belt is preferred.
• Troubleshooting and machine design review.
• Proper communication skills; making complex issues easy for others to understand when acting as a core team member in projects.