CAPA Lead

bdx; El Paso (TX); On-site; USD 90,000 - 130,000; Full time

Job summary

BD, a global leader in medical technology, seeks a CAPA/Quality professional in El Paso to own the site CAPA program and drive regulatory compliance across audits and inspections.

The role requires 5+ years in Quality/Manufacturing within regulated environments, plus 2+ years in CAPA or related leadership. Strong English/Spanish communication and cross-functional collaboration are essential.

Qualifications

• 5+ years in Quality/Manufacturing within a regulated industry (medical device, pharma, or similar).
• 2+ years in CAPA, investigations, or compliance leadership roles.
• Fully bilingual in English and Spanish; strong communication skills.

Responsibilities

• Own and manage the site CAPA program lifecycle from initiation to closure.
• Ensure CAPAs are risk-based, timely, and compliant with regulatory requirements (FDA).
• Lead CAPA governance forums and review boards.
• Drive root cause investigations using methods like 5 Whys, Fishbone, and DMAIC.
• Partner with Operations, Quality, Engineering, and other teams to resolve issues.
• Track CAPA metrics: on-time closure, overdue CAPAs, recurrence, investigation time.

Skills

Bilingual EN/ES

Education

Bachelor’s in Engineering

Tools

CAPA systems

QMS

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:

CAPA Management & Governance

• Own and manage the site CAPA program lifecycle, including initiation, investigation, action planning, implementation, and closure.

• Ensure CAPAs are risk-based, timely, and compliant with internal and regulatory requirements.

• Monitor CAPA effectiveness checks to ensure long-term issue resolution.

• Lead CAPA review boards / governance forums.

Investigations & Root Cause Analysis

• Drive robust problem-solving methodologies (e.g., 5 Whys, Fishbone, Fault Tree, DMAIC).

• Ensure high-quality root cause identification aligned with data and evidence.

• Partner with cross-functional teams (Operations, Quality, Engineering, EHS) to resolve issues.

Compliance & Audit Readiness

• Ensure CAPA processes meet FDA (21 CFR Part 820/210/211 as applicable) and GMP expectations.

• Support regulatory inspections, internal audits, and corporate audits.

• Act as SME for CAPA during audits and inspections.

• Track and report CAPA metrics tied to Warning Letter commitments (if applicable).

Performance Management & Metrics

• Develop and manage CAPA KPIs, including:

• On-time closure rate
• Overdue CAPAs
• Recurrence rate
• Investigation cycle time

• Provide regular reporting to site leadership and corporate teams.

• Identify trends and drive systemic improvements.

Continuous Improvement

• Champion a proactive quality culture focused on prevention vs. correction.

• Integrate CAPA learnings into Lean / BD Excellence initiatives.

• Lead Kaizen or problem-solving events tied to recurring issues.

Training & Capability Building

Train site personnel on:

• CAPA process and expectations
• Root cause analysis tools
• Investigation best practices
• Ensure consistent quality and standardization of investigations across the site.

Education:

• Bachelor’s degree in Engineering, Quality or related field.

Experience:

• 5+ years of experience in Quality/Manufacturing within a regulated industry (medical device, pharma, or similar)

• 2+ years in CAPA, investigations, or compliance leadership roles.

Knowledge and Skills

• Fully Bilingual - English - Spanish

• Strong knowledge of FDA regulations and GMP standards and CAPA systems and quality management systems (QMS)

• Experience with Root cause analysis methodologies, Audit/inspection readiness, Data analysis and trend identification

• Strong cross-functional leadership and influence skills

• Ability to operate in high-pressure, compliance-driven environments

• Excellent communication and executive reporting skills

• Results-driven with strong sense of urgency and accountability

This position is a Fixed Term (limited-term) assignment designed to support a specific business need. Associates in this role are eligible for BD benefits, including medical, dental, health, and 401(k), subject to the eligibility requirements of BD Total Rewards policies. Employment is intended for a defined period and is expected to conclude upon completion of the assignment or fulfillment of the associated business objective

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. 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.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers

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.

Required Skills

Optional Skills

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Primary Work Location

USA TX - El Paso - Northwestern Dr.

Additional Locations

Work Shift