Process Engineer

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

Job Function:

Supply Chain Engineering

Job Sub Function:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Nijmegen, Netherlands

Job Description:

Process Engineer

Are you ready to take on a unique and exciting opportunity as a Process Engineer in the Medical Device Sector? Johnson & Johnson is seeking a highly motivated individual to join our team in Nijmegen, Netherlands with one year limited 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 Process Engineer, you will have the opportunity to work with a team of exceptional professionals and contribute to the success of our goals.

This position reports to the direction of Engineering Manager.

In this job, you 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:

• Ensures workload and priorities of the role are aligned with business need.
• Is accountable for Base Business Activities & engineering projects, including remedial actions when applicable.
• Serves as the engineering reviewer/approver for process development studies and validation documentation in alignment with the Engineering Manager (including CSV).
• Represents engineering department for internal and external communication/reporting/meeting either as a standalone responsibility if applicable or as the Engineering Manager’s delegate.
• Maintains connection with other departments as appropriate.
• Responsible for communicating business related issues or opportunities to next management level.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
• Performs other duties assigned as needed.

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.
• Generally requires (2-4) years related experience.
• Statistical and analytical problem solving.
• 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.
• Manufacturing processes improvements.
• 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.