PHARMAFull-time
Quality Continuous Improvement (CI) Partner, Greater Asia (GA)
MULTIPLE LOCATIONS (APAC) (SG)REMOTEPOSTED: 9/29/2026
PHARMAFull-time
HIRING ORGANIZATIONBECTON, DICKINSON AND COMPANYMedical Technology / Life Sciences
ROLE OVERVIEW
Advanced Quality Continuous Improvement role focused on delivering quality training, coaching and capability building across Greater Asia. The role strengthens quality culture, investigation practices, root cause analysis, continuous improvement and inspection readiness in a regulated life sciences environment.
ROLE DEFINITION & RESPONSIBILITIES
- •Deliver instructor-led, virtual and blended Quality training aligned with enterprise strategy
- •Coach associates, leaders and subject matter experts on Quality processes and compliant behaviours
- •Provide expert coaching on investigations, root cause analysis, problem solving, documentation quality and risk-based decision-making
- •Support audit and inspection readiness, remediation activities, CAPAs and effectiveness checks
- •Identify training gaps and capability needs using data, stakeholder input and observation
- •Develop and enhance training materials, facilitator guides, job aids and capability-building resources
- •Facilitate Kaizen and structured problem-solving activities to drive sustainable improvement
- •Maintain training governance, documentation and records and partner with Quality, process owners and Learning & Development teams
Reporting Hierarchy: Reports to Associate Director, BD Excellence Quality and GPO NC, RCA & PD; Advanced individual contributor; Works cross-functionally with site Quality leaders, process owners, SMEs, Central Quality and Learning & Development
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree in Life Sciences, Sciences, Engineering, Quality, Education or related discipline
- 5+ years of experience in a regulated life science, medical device, pharmaceutical, biologics or similar environment
- Experience delivering Quality or technical training in regulated settings
- Familiarity with regulatory expectations such as FDA and ICH
- Experience in coaching, problem solving, continuous improvement and Quality processes
PREFERRED QUALIFICATIONS
- •MBA or equivalent business experience
- •Experience supporting audit and inspection preparation, response readiness or remediation
- •Experience with training effectiveness measurement and verification
- •Strong facilitation, stakeholder management and influence-without-authority skills
REQUIRED VERIFIED SKILLS
Quality systems
Quality assurance
Continuous improvement
Root cause analysis
RCA
Problem solving
Investigations
CAPA
Nonconformance management
Quality training
Inspection readiness
Audit readiness
Regulatory compliance
Documentation control
Risk-based decision-making
Kaizen
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Health and wellness benefits, paid leave, retirement or savings benefits, professional development and company benefits subject to location
The posting does not disclose salary. Compensation should therefore be evaluated against the applicable Greater Asia location, senior Quality/CI experience and regulated medical technology market benchmarks rather than assumed from the job description.
ORGANIZATION CONTEXT & CULTURE
Becton, Dickinson and Company (BD) is a global medical technology company focused on advancing the world of health through medical technology, manufacturing and healthcare solutions.
TEAM SIZE: 70,000+ employees
INDUSTRY: Medical Technology / Life Sciences
Culture: Purpose-driven and globally collaborative environment emphasizing quality, integrity, continuous improvement, cross-functional partnership and capability building.
EXPECTED CAREER ROADMAP
The role can progress toward senior Quality Excellence, Quality systems, continuous improvement, Quality training leadership or regional/global Quality leadership positions, depending on performance, specialization and organizational opportunities.
APPLICATION ADVISORY
Highlight 5+ years of regulated life sciences or medical-device experience; demonstrate measurable Quality improvement outcomes; emphasize RCA, investigations, CAPA and inspection-readiness experience; showcase instructor-led and virtual training delivery; quantify coaching and capability-building impact; demonstrate Kaizen or structured problem-solving experience; be prepared to discuss influencing stakeholders without direct authority and willingness to travel 25-50%.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.