Associate Director Quality Assurance

Becton Dickinson NA; El Paso (TX); On-site; USD 150,000 - 190,000; Full time

Job summary

Becton, Dickinson, and Company in El Paso, Texas seeks an Associate Director of Quality Assurance to lead site manufacturing QA, ensuring compliance with FDA, EU GMP and ISO standards. This role oversees formulation, filling, sterilization processes, and contamination control strategies, partnering with R&D, Regulatory Affairs, and Manufacturing to drive quality strategy and regulatory readiness.

The candidate should have 10+ years in pharma quality, 5+ years in leadership, and strong experience

Qualifications

• Bachelor's degree in Chemical Engineering or Science.
• Master's degree preferred.
• Minimum 10+ years of experience in Quality within pharmaceutical manufacturing.
• Minimum 5+ years in leadership roles with direct people management responsibility.
• Strong experience with FDA inspections and regulatory interactions (e.g., 483s, Warning Letters).

Responsibilities

• Provide independent Quality oversight of manufacturing operations.
• Drive risk-based decision-making and continuous improvement.
• Lead and develop a high-performing QA organization.
• Act as QA SME during internal and external regulatory inspections.
• Manage budget, resources and priorities for quality site leadership.

Skills

FDA inspections experience

Regulatory interactions

Quality leadership

cGMP knowledge

Risk management

Education

Bachelor's degree in Chemical Engineering or Science

Master's degree preferred

Tools

SAP

Lean/Six Sigma

Job description

We are the people who give possibilities purposeBD 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

The Associate Director, Quality Assurance provides strategic leadership and oversight of the site Manufacturing Operations to ensure compliance with the applicable regulations such as: FDA regulations (21 CFR Parts 210, 211, and 820 as applicable), EU GMP, and ISO 13485 standards.This role is accountable for Quality oversight across the manufacturing process of formulation, filling, triton and Cascade Water Sterilization process (CWS). The position supports and oversight contamination control strategies, risk-based decision-making, and sustainable compliance culture, while enabling operational excellence and supply continuity.The Associate Director acts as a key member of the site quality leadership team, driving quality strategy, regulatory readiness, and continuous improvement initiatives aligned with global and site objectives.Works collaboratively with Manufacturing, Supply Chain, EHS, Engineering, and other cross-functional teams.

Job Responsibilities

Operations Quality Oversight

Ensure adherence to cGMP requirements (21 CFR 210/211, 820 as applicable), EU GMP, and ISO standards. Provide independent Quality oversight of manufacturing operations, including: In-process controls and testing Batch record review and approval Ensure timely disposition decisions based on sound risk assessment and regulatory requirements. Drive increased Quality presence on the shop floor to ensure real-time compliance and issue resolution. Ensure production and process controls are aligned with validated states and lifecycle requirements. Ensure all investigations, CAPA, deviations, change control, complaints, in your area of responsibility are effectively implemented, sustainable, and inspection-ready. Maintain proactive and effective communication with R&D, Design, Regulatory Affairs, and Pharma stakeholders.

Compliance, Risk Management & Continuous Improvement

Drive risk-based decision-making using quality risk management principles. Analyze trends across investigations, complaints, and process performance to identify systemic issues and drive improvements. Leads the development and documentation of structured, data-driven analyses to support root cause identification, decision-making, and continuous improvement initiatives. Serves as the QA Subject Matter Expert (SME) during internal and external regulatory inspections, ensuring accurate representation of quality systems and compliance posture. Ensure effectiveness of CAPAs through robust verification of effectiveness (VoE). Defines and anticipates data requirements, including non-standard datasets, and ensures the collection of robust, high-quality data to support the evaluation of complex issues and operational challenges. Leverages hypothesis-driven analysis and deep understanding of cause-and-effect relationships to evaluate complex processes, identify trends, and interpret data patterns. Serves as a Subject Matter Expert (SME) in leading and documenting comprehensive, data-driven situational analyses to support strategic decision-making, regulatory compliance, and continuous improvement initiatives.

Leadership & Talent Development

Lead, coach, and develop a high-performing QA organization, ensuring appropriate capability across operations and quality systems. Establish clear accountability, drive ownership, urgency, and execution discipline across the team. Develop succession plans and ensure organizational readiness to sustain compliance. Foster a culture of quality, transparency, and continuous improvement.

Business & Strategic Contribution

Act as a key contributor to the quality site leadership team, aligning quality strategy with business objectives. Manage departmental budget, resources, and priorities to ensure effective deployment aligned with business needs and compliance risks.

Education and Experience:

• Bachelor's degree in Chemical Engineering or Science.
• (Master's Degree preferred).
• Minimum 10+ years of experience in Quality within pharmaceutical manufacturing experience.
• Minimum 5+ years in leadership roles with direct people management responsibility.
• Strong experience with FDA inspections and regulatory interactions (e.g., 483s, Warning Letters).

Knowledge and Skills:

• Experience in interface with Domestic and Foreign government agencies
• Experience with SAP preferred
• Experience in Lean/Six Sigma preferred
• Computer proficiency in Microsoft Office (Word, Excel, Power Point, Project, and Outlook).
• Pharmaceutical experience is a must.

Physical Demands:

• Must be able to lift, push/pull, and carry up to 25 pounds
• Must be able to wear appropriate personal protective equipment as required
• Position requires sitting or standing for long hours
• Use of hands and fingers to manipulate office and calibration equipment is required

Work Environment:

Manufacturing

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 SkillsOptional Skills.

Primary Work Location

USA TX - El Paso - Northwestern Dr.