Process Quality Engineer – Manufacturing Analytics

ThermoFisher Scientific; Bedford (MA); On-site; USD 34,000 - 50,000; Full time

Benefits offered by this job

Annual incentive plan bonus

Healthcare

401(k) retirement plan

Paid time off and holidays

Employee stock purchase plan

Job summary

Thermo Fisher Scientific in Bedford, MA is seeking a manufacturing specialist to support high-quality production and process analytics in the Bioproduction division. The role emphasizes problem solving, SOP improvements, and cross-functional collaboration to ensure compliant manufacturing of chromatography media.

You'll lead root cause investigations, revise procedures, train teammates, and adhere to EH&S and ISO13485 standards while contributing to continuous improvement initiatives.

Qualifications

• Bachelor’s degree in Engineering/Science (preferably Chemical Engineering), required or preferred.
• 1 year of Chemical/Operations/Manufacturing or regulated environment experience preferred.
• Experience with SAP or similar inventory control systems is desired.

Responsibilities

• Address and report problems in daily manufacturing and propose effective countermeasures.
• Complete projects as assigned and achieve high-quality results.
• Lead root cause investigations and implement corrective and preventive actions to drive continuous improvement.
• Revise SOPs to enhance processes and readability, minimizing deviations.
• Proactively identify areas for improvement and drive efficient results.
• Execute manufacturing protocols accurately with limited supervision.

Skills

Analytical skills

Troubleshooting

Communication skills

Excel knowledge

Leadership

Training others

Safety compliance

Education

Bachelor's degree in Engineering/Science (preferably Chemical Engineering)

High school diploma or equivalent

Tools

SAP

Job description

Thermo Fisher Scientific in Bedford, MA is seeking a manufacturing specialist to support high-quality production and process analytics in the Bioproduction division. The role emphasizes problem solving, SOP improvements, and cross-functional collaboration to ensure compliant manufacturing of chromatography media.

You'll lead root cause investigations, revise procedures, train teammates, and adhere to EH&S and ISO13485 standards while contributing to continuous improvement initiatives.