Job Description Summary

The Supplier Quality Engineer will contribute to managing the supplier base where the contractual relationship rests with BDCH.

Through proactive communication, effective problem-solving, and active vigilance on applicable requirements, the Associate will ensure product quality and compliance with all relevant global regulations, BD requirements, and customer expectations.

Associate is expected to support a portfolio of suppliers that provide finished goods and will work closely with the Quality and Regulatory representatives within the Regions and Business Units.

The associate will display a desire to deliver quality assurance through supplier management, while putting the customer at the center of everything they do.

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.

Why join us?

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

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.

Become a maker of possible with us!

Our vision for Medication Delivery Solutions at BD

As a leading manufacturer and supplier of products that are used daily in healthcare, the Medication Delivery Solutions (MDS) team provide a wide range of products for injection and infusion therapy, regional anaesthesia and closed medication management.

About the role

As a key member supporting BD Switzerland, the Associate will play a vital role in managing a portfolio of finished goods suppliers under the contractual oversight of BDCH. This role involves maintaining strong relationships with suppliers, ensuring alignment with BD’s quality standards and global regulatory requirements, and proactively resolving issues to uphold product quality and compliance. The Associate will work closely with Quality and Regulatory teams across regions and business units, demonstrating a customer-centric approach and a commitment to continuous improvement in supplier performance.

The Associate will contribute to the development and execution of supplier qualification and requalification processes, support the execution of the supplier audit schedule, and participate in ongoing quality improvement initiatives. A solid working knowledge of key standards such as ISO 13485:2016, MDSAP, MDR, and other applicable ISO standards is essential. This position requires effective communication, strong problem-solving skills, and a proactive mindset to ensure suppliers meet BD’s rigorous quality and compliance expectations.

Main responsibilities will include:

• Support the development and maintenance of supplier qualification/re-qualification activities for the BDCH supplier base.

• Support Supplier Audit Schedule and ensure that audits are carried out as per procedures.

• Support ongoing Quality Improvement projects and initiatives, as required.

• Maintain a detailed and practical knowledge and understanding of ISO13485:2016, MDSAP, MDR and ISO Standards.

• Perform other duties as assigned.

About you

• Engineering / Science degree or Valid Experience in the field.

• Awareness of worldwide applicable regulations for Quality Systems (EU MDR, ISO13485, 21CFR820 etc.) (preferred)

• Experience of working within quality processes such as CAPA, Complaint Management, Risk Management (preferred)

• Experience of conducting audits to international standards such as ISO 9001:2015 and ISO 13485:2016.

• An individual in this role must have results oriented, organization and time management skills with a strong orientation on processes.

• The ability to communicate efficiently in an international environment with external partners and key stakeholders.

Click on apply if this sounds like you!

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully 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 protected status.

To learn more about BD visit: https://bd.com/careers

Required Skills

English Writing, ISO 13485 Medical Devices, Quality Management Systems (QMS), Supplier Auditing, Supplier Qualification, Supplier Quality Management

Optional Skills

Problem Solving, Quality Improvement, Risk Management, Technical Writing

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Primary Work Location

GBR Winnersh - Eskdale Road

Additional Locations

Work Shift