Manufacturing Engineer

About Med Tech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered. Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

We are searching for the best Manufacturing Engineer I This role requires understand of manufacturing processes, preferably having direct experience in a medium to large scale manufacturing companies, with New product introduction (NPI), manufacturing process improvement, capacity expansions and change management competencies. Excellent communication skills and the ability to work with a cross functional team is critical.

• Support the development of business cases for NPI Capital requests.
• Support new asset purchasing and commissioning; work with OEM equipment manufacturers and distributors to develop user requirements.
• Provide technical support in the development and implementation of advanced manufacturing technologies.
• Work with cross-functional teams (Operations Value Stream, OpEx, Planning, Engineering, and Quality) to:
  Align on validation strategy.
• Author validation documents.
• Coordinate execution and document approvals.
• Work with cross-functional teams to:
  Align on implementation plans.
• Lead implementation.
• Provide Manufacturing Engineering (ME) support through stabilization.
• Ensure compliance with: U.S. Food and Drug Administration (FDA) regulations.
• Other regulatory requirements.
• Company policies, operating procedures, processes, and task assignments when supporting projects.
• Perform assignments designed to further develop professional knowledge and abilities, including:
  Application of standard engineering techniques, procedures, and criteria.
• Engineering tasks.
• Project management.
• Statistical analysis.
• Data presentation.
• Technical writing.
• Maintain positive and cooperative communication and collaboration with all levels of employees, customers, contractors, and vendors.
• Ensure all changes are conducted to the highest standards in a safe, compliant, and effective manner.

• A minimum of a Bachelor’s degree in Engineering or Science is required.
• A consistent track record of leading significant change initiatives that have delivered results for an organization is required.
• A minimum of 1–2 years of manufacturing engineering experience is required.
• Understanding of Lean or Six Sigma is preferred.
• Experience working in a regulated industry is required;
  Medical Device experience is preferred.

The role requires on-site presence.