Pharma Process Engineer — Lean Improvement & Compliance

bdx; El Paso (TX); On-site; USD 85,000 - 105,000; Full time

Job summary

BD is a global medical technology company seeking a process-focused engineer to optimize pharmaceutical manufacturing operations in El Paso, TX. You will support validation activities, equipment qualification, and continuous improvement initiatives in a regulated environment.

Responsibilities include leading CAPAs, root-cause investigations, data analysis, and cross-functional collaboration with Quality, Regulatory, and Supply Chain teams.

Qualifications

• Bachelor’s degree in Chemical/Industrial/Mechanical/Biomedical engineering.
• 3+ years of engineering experience in pharmaceutical/medical device/regulated manufacturing.
• Experience in FDA-regulated, 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 complaints.
• Support process validation, equipment qualification, and revalidation activities.
• Lead Lean Manufacturing, Six Sigma, DMAIC projects to reduce waste and improve process capability.
• Coordinate engineering projects from conception to implementation, including timelines and risk assessments.
• Promote safety, compliance, and quality across the site.

Skills

Analytical skills

Root cause investigations

CAPA implementation

Data analysis

MS Office tools

Communication

Collaboration

Education

Bachelor's degree in Chemical Engineering

Bachelor's degree in Industrial Engineering

Bachelor's degree in Mechanical Engineering

Bachelor's degree in Biomedical

3+ years experience in pharma/regulated manufacturing

Tools

SAP

TrackWise

MES

Job description

BD is a global medical technology company seeking a process-focused engineer to optimize pharmaceutical manufacturing operations in El Paso, TX. You will support validation activities, equipment qualification, and continuous improvement initiatives in a regulated environment.

Responsibilities include leading CAPAs, root-cause investigations, data analysis, and cross-functional collaboration with Quality, Regulatory, and Supply Chain teams.