Job Description Summary
Quality Assurance leader for Infusion products platform, responsible for end to end quality systems, development quality and post market quality of the platform products.
Job Description
We are the makers of possible
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.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us.
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Opportunity: Vice President, Quality Assurance, Infusion
Segment: BD Medical
Business: Medication Management Solutions (MMS)
Platform: Infusion Solutions
Role based in San Diego, CA
The Vice President, Quality for the MMS-based Infusion business will be responsible for leading pre and post market quality, including the developing, establishment and maintenance of the quality assurance and engineering programs, policies, processes, procedures and controls during design, development and transfer; ensuring that performance and quality of infusion products globally conform to product requirements, established standards and regulations. This role will lead a team based in San Diego, CA and provide subject guidance for our Eysins, Switzerland and other global sites conducting design and development activities.
This role oversees a varied quality team and is tasked with defining and driving excellent Quality practices, aligned with The BD Way and Quality Management Systems, for:
- Design Assurance and DFX programs
- Design Quality Engineering, including sustaining design change activities
- Software Quality Engineering (embedded, applications and analytics)
- Cybersecurity Risk Management
- Reliability Engineering
- Human Factors Test Method Development and Validation Safety Assurance Case practices.
The Vice President, part of the Multi-functional Infusion Platform Team, will advocate for Quality and Compliance in the Medication Management Solutions (MMS) unit.
The Vice President will ensure that people and processes within the global Design & Development Quality function are capable of active management and improvement of product quality and compliance. As the San Diego site operates under a Consent Decree, the Vice President must align with the conditions outlined in the decree. This position is responsible for significant portions of QMS and product remediation activities within the business. This position reports to the VP of MMS Quality Management and is on the succession path for functional leadership.
The Vice President, Quality Assurance, Infusion will help drive the MMS business strategy as follows:
- Product Risk Management - this position is responsible for the effectiveness of MMS Quality Management System and continued reduction of risks inherent in MMS products and services. As such, defining and maintaining a comprehensive Risk Management Program for all products is required and for Safety Assurance Cases, where required. Included here are full responsibility for software and cybersecurity quality practices. This role involves recognizing how design flaws can affect our collaborators through field feedback data and introducing measures to minimize and improve the quality.
- Design Controls Compliance - this position is responsible for ensuring the MMS Quality Management System elements affecting design and development are effective and efficient enabling risk control and reduction. Compliance to requirements is a must. This leader shall be proficient in the development of design process requirements and leading the organization through the necessary diligence and decisions related to conformance to those requirements throughout the product development life cycle.
- Design Excellence-While quality principles are well-founded in our industry, the position is responsible for identifying superior processes to enable compliance and suitable product quality levels. Critical-To-Quality initiatives will be the driving force behind focusing this team on the critical characteristics of MMS products.
Responsibilities:
- This leader must develop strategic quality programs to oversee and foster: Design changes, New Products, product enhancements, material changes, software creation and maintenance and represent Design Controls expert-level leadership and guidance for a dedicated team.
- This role is a highly matrixed and influential role having responsibility for a broad global portfolio of infusion products' design and development quality practices. As such, this leader must be mature in their understanding and execution of: development of teams including succession planning, organization design and deployment, cross-functional influence and negotiation, and broad organizational change management.
- Define and influence a global quality culture that enables both rapid transformation of ideas to requirements to products and diligent and deliberate compliance to internal quality management system requirements in design and developing them.
- MMS BU-wide authority and accountability for developing, deploying, and maintaining a robust and compliant quality management system for the design, risk management, and ongoing life-cycle maintenance of BD products.
- Actively identify improvements to the processes within the QMS to enhance both compliance and quality.
- Provide expert-level understanding of design control requirements and how to deploy them in a large-scale and rapidly evolving business.
- Provide Design and Development leadership during FDA and Notified body site inspections.
- Interface with the FDA on Pre-Market Activities: Design Controls, Risk Management, Test Methods, Safety Assurance Case, Human Factors
- Acquire and develop excellent-level leaders and teams to support the MMS mission and actively manage bench-strength and succession planning.
- Represent the Quality Function in all product planning activities, such as the Platform Development Team (PDT)
- Identify Quality Initiatives to address field Quality issues, define prevention mechanisms for future development projects and lead cross-functional teams to complete them.
- Provide diligent and fact-based communication to Executive Management team, peers, and team.
- Assess resource needs to align the required level of quality support provided when needed with suitable competencies, including shifting resources between Platforms when appropriate.
- Uphold effective design-related Quality Metrics and define and complete activities to improve performance. Actively support and demonstrate the BD values in daily work.
- Post Market Quality
- Efficiencies in complaint handling
- Build service quality capabilities
- Other assignments as directed by the MMS VP of Quality.
Requirements:
- A BS degree in a technical field (Engineering, Science, Math/Stat)
- Prior leadership experience in Infusion Systems or other durable goods capital equipment medical products.
- At least 20 total years' experience, with at least 15 years' experience leading a Quality Engineering Team in the Medical Device Industry supporting Class II/III devices
- Demonstrated expert-level knowledge of Design Controls, Design for Six-Sigma, Critical-to-Quality strategies, Risk Management, Cybersecurity, Safety Assurance Cases, and Human Factors, etc.
- Demonstrated knowledge of mechanical and electrical engineering in the development of complex devices
- Demonstrated knowledge in Software development lifecycle, including familiarity with embedded software and firmware, applications software and analytics; knowledge of software quality for mobile device apps and remote installation is a plus
- Ability to travel domestically and internationally, up to 25%
- Strong leadership skills with demonstrated ability to deliver excellent results
- Strong project management, team skills, and influential management also highly desired
- ASQ certifications CQE, CSQE, CRE, CMQ/OE, CSSGB and/or CSSBB highly desired.
- Experience leading or supporting FDA and/or Notified Body inspections
- Broad experience with complex, electromechanical, and software devices
- Excellent communication skills (up, down, and outward)
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
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Why Join Us?
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day.
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 health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
To learn more about BD visit https://bd.com/careers
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not discriminate on the basis of 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, or any other legally-protected status.
Required Skills
Optional Skills
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Primary Work Location
USA CA - San Diego Bldg A&B
Additional Locations
Work Shift
NA (United States of America)
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles.
Salary Range Information
$228,600.00 - $411,500.00 USD Annual