Process Improvement Engineer, Medical Devices (Onsite)

Philips; Tennessee; On-site; USD 107,000 - 170,000; Full time

Benefits offered by this job

PTO (Paid Time Off)

401k match

HSA with company contribution

Stock purchase plan

Education reimbursement

Job summary

Philips is seeking an Advanced Manufacturing Engineer for its Bedford, MA site to drive process improvements, validate equipment, and lead continuous improvement initiatives in a regulated medical device environment.

You will partner with production, quality, maintenance, and engineering teams to improve yields, cycle times, and product quality while developing robust manufacturing documentation and procedures.

Qualifications

• 5+ years of experience in manufacturing operations, process validation, production engineering, or related engineering functions in manufacturing.

Responsibilities

• Support daily manufacturing operations by troubleshooting production processes and equipment issues, identifying root causes, and implementing corrective actions to minimize downtime and improve productivity.

Skills

Root Cause Analysis

Process Troubleshooting

Continuous Improvement

Manufacturing Process Development

Equipment Qualification

Process Validation

IQ/OQ/PQ

Lean Manufacturing

Six Sigma

Statistics/Data Analytics

Python

SQL

Power BI

AI Tools / Digital Manufacturing

Education

Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Chemical Engineering, Biomedical Engineering, or related

Tools

Python

SQL

Power BI

Job description

Philips is seeking an Advanced Manufacturing Engineer for its Bedford, MA site to drive process improvements, validate equipment, and lead continuous improvement initiatives in a regulated medical device environment.

You will partner with production, quality, maintenance, and engineering teams to improve yields, cycle times, and product quality while developing robust manufacturing documentation and procedures.