Becton Dickinson logo

Quality Excellence Capability Specialist

Becton Dickinson

Franklin Lakes, NJ; Tempe, AZ; Covington, GA; San Diego, CA; Sandy, UT; Salt Lake City, UTHybridPosted 1 day ago$135,500 - $216,800/year
Full TimeMid LevelQuality (QA / QC)Medical Device
Original posting ↗

Summary

The Quality Excellence Capability Specialist supports the deployment and day-to-day execution of BD's Quality Excellence Academy. The primary focus is coordinating training schedules, partnering with sites to plan learning activities, managing logistics and communications, and maintaining documentation needed for effective and compliant program execution.

Job description

Position Summary

The Quality Excellence Capability Specialist supports the deployment and day-to-day execution of BD's Quality Excellence Academy. The primary focus is coordinating training schedules, partnering with sites to plan learning activities, managing logistics and communications, and maintaining documentation needed for effective and compliant program execution.

Key Responsibilities

  • Coordinate deployment of Quality Excellence Academy learning activities in alignment with regional plans and priorities.
  • Partner with site Quality contacts to coordinate training needs, target audiences, schedules, delivery formats, language considerations, and logistical requirements.
  • Maintain regional training calendars, site schedules, participant rosters, completion records, action logs, and other program documentation.
  • Coordinate instructor and subject matter expert availability, virtual meeting logistics, training materials, room requirements, participant communications, and session follow-up.
  • Co-lead instructor-led, virtual, and blended learning sessions with Quality Excellence Capability Partners, process owners, or qualified subject matter experts.
  • Deliver selected training sessions independently on an occasional basis after completing required qualification, preparation, and content familiarization.
  • Support capability-building programs in areas such as Investigation Management, Root Cause Analysis, Problem Solving, Process Validation, Change Control, Technical Writing, and other quality priorities.
  • Prepare and organize facilitator guides, participant materials, exercises, assessments, and supporting resources using approved content.
  • Collect participant feedback and assessment results and summarize themes, issues, and improvement opportunities for program leads.
  • Provide clear, timely status updates on upcoming sessions, site readiness, participation, completion, scheduling risks, and follow-up actions.

Additional Responsibilities

  • Partner with site Quality teams, regional Quality Excellence Capability Partners, Central Quality, Learning & Development, and business stakeholders to support consistent program execution.
  • Maintain accurate and complete records associated with training delivery, learner participation, qualification, and effectiveness activities in accordance with applicable requirements.
  • Support training effectiveness activities through surveys, assessments, observations, stakeholder feedback, and follow-up tracking.
  • Use training data, quality metrics, audit or inspection observations, and stakeholder feedback to help identify recurring capability needs and scheduling priorities.
  • Support onboarding, targeted remediation, CAPA-related learning activities, and other focused capability-building efforts as assigned.
  • Assist with Kaizen events, structured problem-solving workshops, community-of-excellence activities, and sharing of best practices across sites.
  • Identify opportunities to simplify coordination, improve the learner experience, strengthen documentation, and increase consistency across regions.
  • Promote a culture of continuous learning, accountability, quality excellence, and operational effectiveness.

Education and Experience Required

  • Bachelor's Degree in Life Sciences, Sciences, Engineering, Education, Business, Operations, or a related field is required.
  • 3+ years of relevant experience in medical device, pharmaceutical, biologics, manufacturing, quality, learning and development, or another regulated environment.
  • Experience coordinating training, projects, programs, events, or cross-functional activities involving multiple stakeholders, locations, or time zones.
  • Working knowledge of regulated quality systems and quality processes such as CAPA, nonconformance management, investigations, change control, process validation, design controls, or risk management.
  • Experience supporting or delivering instructor-led or virtual training, presentations, workshops, or other learning activities.
  • Strong organizational and planning skills, with demonstrated attention to detail and the ability to manage multiple schedules, priorities, and follow-up actions.
  • Strong written and verbal communication skills, with the ability to engage associates, facilitators, subject matter experts, and site leaders.
  • Proficiency with Microsoft 365 tools used for scheduling, communication, tracking, collaboration, and presentation development.
  • Ability to work effectively in a matrixed, cross-functional, and multicultural environment.
  • Willingness to travel domestically and internationally as required, approximately 25%.

Preferred Knowledge and Experience

  • Ability to communicate and deliver training in Spanish is preferred.
  • Experience supporting teams or sites globally is preferred.
  • Experience using a learning management system or maintaining controlled training records is preferred.
  • Experience with adult learning principles, facilitation, learner engagement, or training effectiveness is preferred.
  • Experience supporting audit readiness, inspection readiness, remediation, or quality improvement activities is preferred.
  • Experience with problem-solving, continuous improvement, Lean, or Kaizen methods is preferred.
  • Ability to adapt communication and coordination approaches across different cultures, languages, and organizational levels.

Requirements

  • Bachelor's Degree in Life Sciences, Sciences, Engineering, Education, Business, Operations, or a related field
  • 3+ years of relevant experience in medical device, pharmaceutical, biologics, manufacturing, quality, learning and development, or another regulated environment
  • Experience coordinating training, projects, programs, events, or cross-functional activities involving multiple stakeholders, locations, or time zones
  • Working knowledge of regulated quality systems and quality processes such as CAPA, nonconformance management, investigations, change control, process validation, design controls, or risk management
  • Experience supporting or delivering instructor-led or virtual training, presentations, workshops, or other learning activities
  • Strong organizational and planning skills
  • Strong written and verbal communication skills
  • Proficiency with Microsoft 365 tools
  • Ability to work effectively in a matrixed, cross-functional, and multicultural environment
  • Willingness to travel domestically and internationally approximately 25%

Benefits

  • Medical, Dental & Vision
  • Health Savings Accounts
  • Flexible Spending Accounts
  • Life & AD&D Insurance
  • Short & Long-Term Disability
  • 401(k) Matching
  • Deferred Compensation Plan
  • 529 College Savings Plan
  • Paid Time Off
  • Paid Parental Leave
  • Adoption Assistance
  • Tuition Reimbursement
  • Employee Assistance Program
  • Commuter Benefits
  • Pet Insurance
  • Backup Childcare & Eldercare
  • Wellness Programs
  • Financial Counseling
  • DailyPay

Company overview

Becton, Dickinson and Company (BD) is a leading American multinational medical technology company founded in 1897 and headquartered in Franklin Lakes, New Jersey. As one of the largest global medical technology companies, BD specializes in manufacturing and selling medical devices, instrument systems, and reagents while also providing consulting and analytics services. The company operates through three main segments: BD Medical (focusing on medication delivery and management), BD Life Sciences (specializing in diagnostics and biosciences), and BD Interventional (concentrating on surgical and critical care interventions). With over 72,000 employees worldwide, BD has established a significant presence in virtually every country and serves healthcare providers, hospitals, clinics, pharmaceutical companies, and research institutions. The company is publicly traded on the New York Stock Exchange (NYSE: BDX) and is a component of the S&P 500 index. BD has a long history of innovation, including developing the first insulin injection device in 1924, the first sterile disposable medical device in 1952, and pioneering safety-engineered syringes. The company continues to advance healthcare through its commitment to improving medical discovery, diagnostics, and care delivery while addressing global health challenges.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.