Process Engineer - Lean, Validation & Improvement

BD; El Paso (TX); On-site; USD 85,000 - 130,000; Full time

Job summary

BD is seeking an experienced Process Engineer to support pharmaceutical manufacturing. The role focuses on optimizing processes, validating equipment, and driving continuous improvement within a highly regulated environment.

You will work closely with cross-functional teams to ensure quality, compliance, and timely project delivery. Ideal candidates have a solid background in chemical/industrial/mechanical engineering, expertise in validation, and proficiency with manufacturing systems like SAP,

Qualifications

• Bachelor’s degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, or Biomedical.
• 3+ years in pharmaceutical/medical device manufacturing or highly regulated environments.
• Experience with FDA regulations, cGMP, validation, and quality systems.

Responsibilities

• Provide day-to-day engineering support to pharmaceutical manufacturing operations.
• Analyze manufacturing processes to identify opportunities for efficiency, quality, yield and cost improvements.
• Lead CAPAs and root cause investigations for process deviations and customer complaints.
• Monitor process performance using data analysis and KPIs.
• Support process validation, equipment qualification (IQ/OQ/PQ), and revalidation activities.
• Coordinate engineering projects for new product introductions, technology transfers, and process changes.
• Promote safety, compliance, and quality in all engineering activities.

Skills

Analytical skills

Root cause analysis

Data analysis & MS Office

Education

Bachelor’s degree in Chemical Engineering

Bachelor’s degree in Industrial Engineering

Bachelor’s degree in Mechanical Engineering

Bachelor’s degree in Biomedical

Tools

SAP

TrackWise

MES

Job description

BD is seeking an experienced Process Engineer to support pharmaceutical manufacturing. The role focuses on optimizing processes, validating equipment, and driving continuous improvement within a highly regulated environment.

You will work closely with cross-functional teams to ensure quality, compliance, and timely project delivery. Ideal candidates have a solid background in chemical/industrial/mechanical engineering, expertise in validation, and proficiency with manufacturing systems like SAP,