Pharma Process Engineer: Tech Transfer & QbD

Bimeda, Inc.; Pomona (CA); On-site; USD 110,000 - 165,000; Full time

Benefits offered by this job

401(k) plan

Paid time off

Life insurance

Employee assistance program

Job summary

Bimeda is seeking a Process Engineer for in-office work in Pomona, CA. You will lead technology transfer, scale-up, and validation activities across manufacturing processes, partnering with production, quality, and validation teams to ensure compliant, robust operations.

The role emphasizes QbD, risk assessment, and data-driven optimization to improve process performance, product quality, and manufacturing efficiency. A strong background in chemical engineering and GMP is required.

Qualifications

• Bachelor’s degree in Chemical Engineering with 4+ years of relevant experience.
• Master’s degree in Engineering or related discipline with 2+ years of relevant experience.

Responsibilities

• Lead technology transfer activities for commercial products and develop transfer protocols and reports.
• Coordinate pilot, engineering, and validation batches with cross-functional teams.
• Develop process flow diagrams and technical documentation to support manufacturing.
• Apply QbD principles to ensure scalable, reproducible processes meeting quality requirements.
• Lead or support equipment qualification and process improvement initiatives.
• Provide technical leadership for deviations, CAPAs, and Change Controls.

Skills

Technology transfer

Process scale-up

Validation

Quality by Design (QbD)

GMP compliance

Education

Bachelor’s degree in Chemical Engineering

Master’s degree in Engineering

Job description

Bimeda is seeking a Process Engineer for in-office work in Pomona, CA. You will lead technology transfer, scale-up, and validation activities across manufacturing processes, partnering with production, quality, and validation teams to ensure compliant, robust operations.

The role emphasizes QbD, risk assessment, and data-driven optimization to improve process performance, product quality, and manufacturing efficiency. A strong background in chemical engineering and GMP is required.