Process Engineer - Pharma

BD; El Paso (TX); On-site; USD 75,000 - 110,000; Full time

Job summary

BD is seeking an experienced Process Engineer to provide day-to-day support for pharmaceutical manufacturing operations in El Paso, TX. You will analyze process performance, lead CAPA investigations, and drive Lean Six Sigma initiatives to improve efficiency, quality, and cost.

Responsibilities include supporting validation, equipment qualification, audits, and regulatory commitments while collaborating with cross-functional teams to maintain rigorous safety and quality standards in a highly

Qualifications

• Bachelor's degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Biomedical.
• 3+ years of engineering experience in pharmaceutical/medical device/regulated manufacturing.
• Experience with FDA/cGMP/validation and quality systems.

Responsibilities

• Provide day-to-day engineering support to pharmaceutical manufacturing operations.
• Analyze processes to improve efficiency, quality, yield and cost.
• Lead root cause investigations and implement CAPAs.
• Support process validation, equipment qualification, and revalidation activities.

Skills

Analytical skills

Root cause & CAPA

Data analysis tools

Education

Bachelor's degree in Chemical Engineering or related field

Lean Six Sigma Green/Black Belt

Tools

SAP

TrackWise

MES

Job description

We Are The People Who Give Possibilities Purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Responsibilities Include But Are Not Limited To

Process Optimization & Manufacturing Support

• Provide day-to-day engineering support to pharmaceutical manufacturing operations.
• Analyze manufacturing processes to identify opportunities for improving efficiency, quality, yield, and cost.
• Troubleshoot process issues and implement corrective and preventive actions (CAPAs).
• Monitor process performance through data analysis and key performance indicators (KPIs).
• Lead root cause investigations related to process deviations, nonconformances, and customer complaints.

Validation & Compliance

• Support process validation, equipment qualification, and revalidation activities.
• Develop and execute validation protocols, reports, and technical documentation.
• Ensure compliance with FDA regulations, cGMP requirements, BD policies, and applicable quality standards.
• Support internal and external audits, inspections, and regulatory commitments.
• Maintain manufacturing documentation, standard operating procedures (SOPs), and work instructions.

Continuous Improvement

• Lead Lean Manufacturing and Continuous Improvement projects.
• Utilize Six Sigma, DMAIC, and problem-solving methodologies to eliminate waste and improve process capability.
• Identify and implement productivity, quality, and cost-reduction initiatives.
• Participate in site transformation and operational excellence programs.

Project Management

• Support new product introductions, technology transfers, and process changes.
• Coordinate engineering projects from conception through implementation.
• Manage timelines, risk assessments, resource requirements, and project documentation.
• Collaborate with Maintenance, Quality, Operations, Validation, Regulatory Affairs, and Supply Chain teams.

Safety & Quality

• Promote a strong culture of safety, compliance, and quality.
• Support risk assessments, process hazard evaluations, and quality improvement initiatives.
• Ensure all engineering activities are performed following EHS and Quality Management System requirements.

Education And Experience

• Bachelor’s degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Biomedical
• 3+ years of experience of engineering experience within a pharmaceutical, medical device, biotechnology, or highly regulated manufacturing environment
• Experience working in FDA-regulated, cGMP, validation, and quality systems.
• Experience in pharmaceutical manufacturing and aseptic or sterilization processes preferred.
• Knowledge of process validation, equipment qualification (IQ/OQ/PQ), and risk management methodologies, preferred.
• Lean Six Sigma Green Belt or Black Belt certification preferred.
• Experience with SAP, TrackWise, MES, or other manufacturing systems preferred.
• Knowledge of statistical tools and process capability analysis.
• Bilingual (English/Spanish) preferred.

Knowledge And Skills

Technical Skills

• Strong analytical and problem-solving skills.
• Experience conducting root cause investigations and implementing CAPAs.
• Proficiency in Microsoft Office applications and data analysis tools.

Key Competencies

• Strong problem-solving and analytical skills
• Detail-oriented with data-driven decision making
• Ability to manage problem solving and critical thinking
• Effective communication and collaboration across all levels

Physical Demands

• Manufacturing environment with exposure to production areas.

Work Environment

• Manufacturing

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Primary Work Location

USA TX - El Paso - Northwestern Dr.