Process Engineer II , Orthopedics

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.

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 https://www.jnj.com/medtech

"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.”

• →B.S Engineering Degree or Science Discipline
• →Approximate experience, or equivalent knowledge and skills, necessary to satisfactorily perform the position responsibilities. 2 to 4 years’ experience in manufacturing/design engineering.

• →Six Sigma Green Certification and/or other project management methodology is preferred.
• →Able to read and understand engineering drawings and translate product drawings into process information
• →Hands on experience with manual assembly equipment and/or processes
• →Position requires excellent organizational and communication skills (written and oral, fluent in English)
• →Ability to make and manage good relationships
• →Presentation skills
• →Analytical and problem-solving skills
• → Initiative and results/target focused
• →An understanding of Lean Manufacturing and lean principles with an ability to promote and drive continuous improvement
• →Understanding of design and production costs to include waste, downtime, scrap and re-work
• →Understanding of calibration concepts and Measurement systems.
• →Experience with the essential requirements of the Medical Device Directive (MDD), ISO 13485, FDA design controls or similar regulatory environment in design control and process validation
• →Experience on medical device (Class II or Class III) projects.
• →Experience utilizing enterprise resource planning (ERP) tools.
• →Understanding of customer expectations and deliverables with an awareness of the impact of failure/cost of poor quality