Process Engineer
Becton Dickinson Medical Devices•El Paso, TX
•Onsite
About The Position
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.
Requirements
- 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.
- Knowledge of statistical tools and process capability analysis.
Nice To Haves
- 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.
- Bilingual (English/Spanish) preferred.
Responsibilities
- 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.
- 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.
- 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.
- 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.
- 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.
Benefits
- culture where face-to-face collaboration supports your learning, your progress, and your success.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
