Process Engineer II — MedTech Manufacturing

Johnson & Johnson MedTech; Raynham (MA); On-site; USD 65,000 - 105,000; Full time

Job summary

Johnson & Johnson is seeking a Process Engineer for its DePuy Synthes Joints Platform manufacturing innovation team in Raynham, MA. The role focuses on developing, validating, and optimizing manufacturing processes to enhance quality and efficiency.

Collaborate with Operations, Quality, Engineering, and Supply Chain to apply DOE, CAPA, and continuous improvement in a regulated medical device setting within a large global company.

Qualifications

• Bachelor's degree in engineering or equivalent technical discipline.
• 2-4 years of engineering experience in manufacturing or process engineering.
• Experience in a regulated industry such as Medical Device or Pharmaceutical.

Responsibilities

• Support the development, implementation, and optimization of manufacturing processes, equipment, and controls to improve quality, efficiency, and operational performance.
• Conduct process characterization, capability studies, DOE, and data analysis to improve understanding and performance.
• Research current and emerging technologies and evaluate alternatives related to process capability, quality, and cost.
• Collaborate with cross-functional teams on projects involving process improvements, new product introductions, and equipment implementation.
• Provide manufacturability feedback through design reviews and collaboration with teams.

Skills

Analytical skills

CAPA

DOE

Lean Six Sigma

Process control

Gemba Kaizen

GMP awareness

Qualification testing

Education

Bachelor's Degree in Engineering

Tools

Minitab

Microsoft Office

Job description

Johnson & Johnson is seeking a Process Engineer for its DePuy Synthes Joints Platform manufacturing innovation team in Raynham, MA. The role focuses on developing, validating, and optimizing manufacturing processes to enhance quality and efficiency.

Collaborate with Operations, Quality, Engineering, and Supply Chain to apply DOE, CAPA, and continuous improvement in a regulated medical device setting within a large global company.