Process Engineering Tech I

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.
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.
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.
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.
Identify and implement productivity, quality, and cost-reduction initiatives.
Participate in site transformation and operational excellence programs.
Project Management

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.
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.

Manufacturing

We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
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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.
Work Shift