Process Engineer – Pharma Packaging & Process Improvement

Centor; Millersburg (OH); On-site; USD 80,000 - 90,000; Full time

Benefits offered by this job

Healthcare

Prescription drug coverage

Flexible spending accounts

Wellness

Disability coverage

401k match

EAP (Employee Assistance Program)

Life insurance

PTO (Paid Time off)

Holidays

Job summary

Centor is seeking a Process Engineer in Berlin, Ohio to own and improve manufacturing processes, ensure capability and compliance, and collaborate with Quality, Maintenance and Supply Chain. You will drive process stability, cost reduction, and robust validation activities to support GMP-regulated environments.

The role emphasizes cross-functional collaboration, data-driven decision making, and structured problem solving to achieve on-time delivery and quality targets.

Qualifications

• Bachelor's degree in Engineering or related field.
• 2-4 years of process engineering experience in manufacturing.
• Strong knowledge of SPC, Lean/Six Sigma, root cause analysis and process validation.

Responsibilities

• Own and maintain process parameters for all production lines within the assigned building.
• Define standard operating windows and control limits.
• Monitor and improve process capability (Cp, Cpk).
• Ensure process documentation (work instructions, parameter sheets) is current and accurate.
• Provide on-floor technical support during process deviations.
• Drive improvements in OEE, FA/RFT, scrap reduction, and cycle time optimization.
• Lead structured problem-solving using DMAIC, 5-Why, and Fishbone diagrams.
• Implement Lean manufacturing initiatives and reduce CNQ.
• Support validation activities (IQ/OQ/PQ) and change control.
• Conduct risk assessments (FMEA) for new or modified processes.

Skills

SPC

Lean Six Sigma

Root cause analysis

Process validation

Education

Bachelor's degree in Engineering

Job description

Centor is seeking a Process Engineer in Berlin, Ohio to own and improve manufacturing processes, ensure capability and compliance, and collaborate with Quality, Maintenance and Supply Chain. You will drive process stability, cost reduction, and robust validation activities to support GMP-regulated environments.

The role emphasizes cross-functional collaboration, data-driven decision making, and structured problem solving to achieve on-time delivery and quality targets.