Manufacturing Unit Leader- Pharma
BD
El Paso, Texas
Full-Time
Competitive
OfficeManager
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.
The Pharma Manufacturing Unit Leader (MUL) is responsible for leading end-to-end manufacturing operations within the Pharma unit, ensuring strict compliance with regulatory standards (FDA, GMP) while driving operational excellence and delivering business performance targets. This role oversees cross-functional teams to ensure safe, high-quality, and efficient production, aligned with BD’s transformation, compliance remediation, and continuous improvement initiatives.
As a Pharma Manufacturing Leader, this position operates in a highly controlled environment involving chemical and biological products, where risk is directly associated with dose accuracy, product potency, and contamination control. The role places a critical emphasis on robust process control, sterility assurance, and reproducibility to guarantee consistent product quality and patient safety.
Job Responsibilities:
Operational Leadership
Lead end-to-end daily manufacturing operations for the Pharma unit, ensuring strict adherence to production plans, safety protocols, and quality standards.
Provide clear and consistent direction to frontline leaders and production teams across all shifts to ensure alignment and execution discipline.
Drive effective implementation of Tiered Management and Daily Management Systems (TMS) to establish clear priorities and maintain operational control.
Oversee core pharma operations, including formulation, aseptic processing, and filling activities.
Maintain daily focus on:
Deviations and batch disposition
Environmental monitoring and cleanroom compliance
Sterility assurance and contamination control
Operate with a low tolerance for process variation, ensuring consistency and reproducibility.
Manage changes through a highly structured change control process, recognizing that:
Every change carries potential regulatory and validation impact (changes may require re-validation, requalification, or regulatory approval).
Ensure strict adherence to:
Batch record review and documentation practices
QC testing and formal release processes
Oversee operations within highly controlled environments, including:
Cleanroom classifications (Grades A–D)
Environmental and contamination controls
Gowning, airlocks, and facility compliance standards
Recognize that facilities and utilities are integral to process validation and product quality.
Compliance & Quality
Ensure full compliance with FDA regulations, GMP standards, BD Quality Systems, and internal procedures, maintaining an always audit-ready environment.
Lead inspection readiness and actively support regulatory audits (FDA, internal, and external).
Drive timely and effective resolution of deviations, non-conformances (NCRs), and audit findings through robust CAPA processes.
Reinforce a strong quality culture with accountability at all levels, grounded in the principle:
“Follow the process exactly and prove every batch meets specification.”
Maintain focus on critical pharma risks including dose accuracy, potency, and contamination control.
People Leadership & Engagement
Lead, coach, and develop supervisors and production teams to build a high-performing, compliant, and accountable organization.
Ensure adequate staffing, capability building, and succession planning for business-critical roles.
Demonstrate discipline, rigor, and a zero-tolerance mindset for deviations.
Foster a culture of strong governance, documentation excellence, and audit readiness.
Balance operational performance with compliance priorities by:
Driving compliance discipline and deviation reduction
Accepting structured, deliberate decision-making processes
Maintaining focus on contamination control, batch release, and inspection readiness.
Promote BD Values, a strong Speak Up culture, and an inclusive, respectful work environment.
Operational Excellence & Continuous Improvement
Lead Lean and BD Excellence initiatives, including Kaizen events, process standardization, and waste elimination.
Deliver productivity improvements and cost targets aligned with the Cost-to-Win (CTW) strategy.
Leverage KPIs and data analytics to drive performance, with particular focus on deviation reduction, batch release efficiency, and right-first-time execution.
Support Factory Blueprint implementation and sustain standard work practices across the unit
Safety & EHS
Ensure compliance with EHS standards and promote a zero-incident safety culture.
Address risks proactively and lead investigations for safety incidents.
Partner with EHS to drive preventive actions and regulatory compliance.
Cross-functional Collaboration
Partner with Quality, Engineering, Maintenance, Supply Chain, and HR to ensure seamless and compliant operations.
Support new product introductions (NPI), validation activities, and process transfers.
Align resources to meet production and business priorities.
BD Excellence, TMS, and Continuous Improvement
Lead the TMS cycle and set the 24‑hour direction for the Manufacturing Unit.
Sustain BD Excellence through Daily Tier Meetings (DTM), Clean/Inspect/Lubricate (CIL/CL) standards, and loss elimination practices.
Drive short- and long-term improvements aligned with SQDCP (Safety, Quality, Delivery, Cost, People) objectives.
Other Responsibilities
Perform additional duties as required to support the needs of the business and site operations.
Education and Experience:
Bachelor’s Degree in Engineering, Life Sciences, Manufacturing, or related field required. Master’s Degree preferred
5+ years of manufacturing experience in Pharma is required.
Minimum 3–5 years in people leadership roles
Strong experience with FDA regulations, GMP compliance, and audit management
Proven track record in continuous improvement (Lean, Six Sigma preferred)
Flexibility to support multiple shifts and business needs
Ability to work in a fast-paced, highly regulated manufacturing environment.
Knowledge and Skills:
Strong knowledge of pharmaceutical/medical device manufacturing processes
Experience with deviation management, CAPA, and quality systems
Familiar with ERP systems (e.g., SAP, Workday) and production planning tools
Data-driven mindset with ability to analyze and act on performance metrics
Strategic thinking and execution
Strong decision-making and problem-solving skills
Effective communication across all organizational levels
Change management and transformation leadership
Collaboration and influence across cross-functional teams
Work Environment:
On‑site role in a clean, highly regulated, high‑volume medical device/pharma manufacturing facility. Requires interaction with Quality, Production, EHS, Engineering, and Facilities teams.
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 visithttps://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.
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