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Quality Engineer II

In-Office, Singapore, Singapore

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Job ID
R-554507
Category
Engineering
Location
Singapore, Singapore

Build an engineering career where innovation, ownership and impact move healthcare forward

At BD, Engineering and R&D professionals design, develop and improve the technologies that shape how healthcare is delivered worldwide. You'll apply scientific thinking, technical expertise and creative problem-solving to turn complex challenges into solutions that matter.

Whether you specialize in mechanical, electrical, process, systems, software or research engineering, BD offers the scale, resources and freedom to innovate – with clear expectations, accountability for outcomes and opportunities to grow your career alongside industry-leading technology.

And as one of the world's largest medical technology companies, you'll shape solutions that reach across global healthcare systems and improve lives at scale.

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

About the Role

We are looking for a Quality Assurance Engineer to support product development and quality system activities within a regulated medical device environment.

In this role, you will ensure compliance with ISO 13485, FDA Quality System Regulations (21 CFR Part 820), and international regulatory requirements while supporting design control, risk management, and continuous quality improvement initiatives.

You will work closely with cross-functional teams throughout the product development lifecycle to ensure quality and compliance are built into every stage of the process. This role aligns with BD's focus on maintaining robust quality systems, design controls, and regulatory compliance.

What You'll Do

  • Support and maintain Design and Development Controls in compliance with ISO 13485 and FDA Quality System Regulations.
  • Lead or support Risk Management activities in accordance with ISO 14971.
  • Participate in product development projects, ensuring quality assurance deliverables are completed accurately and on time.
  • Create, revise, and maintain controlled quality documentation, including SOPs, specifications, procedures, and test methods.
  • Ensure compliance of R&D and quality system processes with applicable regulatory and customer requirements.
  • Support continuous improvement initiatives to strengthen quality system effectiveness and operational excellence.
  • Apply Six Sigma methodologies and quality tools to improve product development processes.
  • Provide quality system expertise and training to cross-functional teams.
  • Participate in ongoing Quality Assurance and Quality Systems activities, audits, and compliance initiatives.
  • Collaborate with engineering, manufacturing, regulatory, and project teams to ensure successful product development and lifecycle management.

Job Requirements

  • Bachelor's Degree in Mechanical Engineering, Life Sciences, Quality, Biomedical Engineering, or a related discipline.
  • Minimum 2 years relevant experience in a quality role in a medical device company
  • Experience in a R&D Phase-Gate development process and/or design transfer process
  • Experience in Quality Assurance, Design Quality, Quality Systems, or regulated product development environments.
  • Strong knowledge of ISO 13485, FDA 21 CFR Part 820/QSR, and medical device quality system requirements.
  • Working knowledge of Design Controls, Verification & Validation, and Risk Management (ISO 14971).
  • Experience with quality documentation, SOP development, change control, and document management systems.
  • Familiarity with Six Sigma, continuous improvement methodologies, or quality tools is advantageous.
  • Strong problem-solving, analytical, and communication skills.
  • Ability to work effectively in cross-functional teams and manage multiple priorities.
  • Experience supporting audits, regulatory inspections, and compliance activities is preferred.

What's In It For You

  • Competitive full‑time compensation package and benefits
  • Paid company holidays (public holidays, rest days, etc.)
  • Opportunities for career development and growth
  • Convenient company transportation provided

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 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.

Required Skills

Optional Skills

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Primary Work Location

SGP Tuas - Tuas

Additional Locations

Work Shift

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Success Profile

What sets successful Engineering and R&D professionals apart? You're likely to thrive if you are:

  • Analytical
  • Collaborative
  • Curious
  • Detail-oriented
  • Inventive
  • Problem-solver

Ready for your next challenge?

This is an environment for engineers who want to think boldly and execute with precision. You'll have the opportunity to influence design decisions, contribute across the full product lifecycle and see how your work moves from concept to real-world impact – backed by the scale of a global MedTech leader.

Hear from one of our BD Innovators about how BD uses cutting-edge AI and machine learning to power decisions that improve patient outcomes and expand access to care. This is where your work drives real-time impact across the globe.

Hear from Our Associates

  • "BD is a big, global company so don't be afraid to connect with and reach out to others. There is so much to learn here, and the company does an amazing job of helping people develop and grow. I'd also offer to become like a sponge and soak up as much knowledge as you can and put your Career Blueprint to work for you. I really love my job and am so grateful to work at BD."

  • "I think we have something like more than 30 different countries represented by those working within the Research Centre Ireland, which is impressive and one of my favourite things about BD. I work with electrical, mechanical engineers, scientists and so many others – it's wonderful to see and hear so many different perspectives during the day."

  • "I continue to be amazed at how we keep innovating in the Med Tech space. We constantly evaluate how to bring even more solutions to healthcare professionals, how to increase the efficiency of our technologies, all while keeping the patient impact in mind. Not only have I found meaningful work at BD, but a place where I feel I can thrive."

  • "During my interview, I learned how much of an impact our infusion solutions have across the world and I was impressed because whether it's analgesics, cancer treatments, anesthesia or other treatments, the likelihood of someone within your own family using our product is high. Contributing to the creation of products that have the ability to make such a big impact in healthcare is a great feeling. I love my role at BD."

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