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Manager, QA Inspection

Onsite, San Diego, CA

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ID de l'offre
R-542177
Category
Quality
Location
San Diego, Californie
As a result of the combination of the BD Biosciences and Diagnostic Solutions business with Waters Corporation (NYSE: WAT), by applying to this role, you will be applying for a position with Waters. Waters is a global leader in life sciences, dedicated to accelerating the benefits of pioneering science through analytical technologies, informatics, and service. With a focus on regulated, high-volume testing environments, Waters’ innovative portfolio harnesses deep scientific expertise across biology, chemistry, and physics. Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance. Through a shared culture of relentless innovation, Waters’ passionate team of approximately 16,000 colleagues partner with customers to turn scientific challenges into breakthroughs that improve lives worldwide.

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.

Job Description

Job Overview:

Reporting to the Associate Director, QA, the Manager, QA Inspection - Biosciences provides direct management to technical staff in San Diego. This role provides day‑to‑day leadership of QA Inspectors, owns inspection strategies and plans, ensures inspection readiness, and partners closely with Manufacturing, Quality Engineering, and Regulatory teams to support compliant and efficient operations. Through outstanding communication; effective problem solving and active management of ambiguous situations; manager ensures product safety, product quality and compliance with all relevant global regulations and customer expectations. Success is measured in terms of the frequency and scale of product quality organizational issues as well as business process effectiveness. Through stakeholder engagement; and people development; the Manager produces durable and industry leading results supporting key business drivers.

Primary Responsibilities:

  • Lead and manage QA Inspection teams responsible for reagent production.

  • Ensure inspections are driven in accordance with approved procedures, drawings, specifications, and control plans.

  • Establish and maintain staffing plans, shift coverage, training, and qualification of QA Inspectors.

  • Ensure inspection processes align with FDA QSR, ISO 13485, and corporate quality requirements.

  • Support internal, corporate, and regulatory audits/inspections related to inspection controls and product release.

  • Ensure inspection‑related nonconformances are properly documented and raised.

  • Partner with Quality Engineering to support nonconforming material investigations, containment, and disposition.

  • Drive timely closure of inspection‑related CAPAs and effectiveness checks where assigned.

  • Monitor inspection trends and find opportunities for defect reduction and process improvement.

  • Recruit, coach, and develop QA Inspectors and lead inspectors.

  • Set clear expectations, conduct performance reviews, and support skill progression and cross‑training.

  • Foster a culture of quality, accountability, and continuous improvement.

Minimum Requirement:

  • A minimum of a bachelor’s degree in science, engineering, or other relevant discipline with a minimum of five (5) years relevant experience in the pharmaceutical and/or medical device industries, with two (2) years supervisory experience.

  • Experience with GMP/ISO compliance and documentation, and FDA Regulations.

  • Knowledge of manufacturing systems, medical products and related materials, quality testing and quality auditing.

  • Six Sigma or Lean certification desired.

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 Skills

Optional Skills

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Primary Work Location

USA CA - San Diego (BDB)

Additional Locations

Work Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$126,600.00 - $208,900.00 USD Annual
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