QA Technical Specialist

Job Description Summary

Support QA incoming function in manufacturing plant QA function.

**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

A. General Accountability
- Safety and ISO14001 Environmental accountability. Ensure a safe, healthy, and environmentally friendly workplace by observing Company’s rules and procedures. Active involvement in prevention, elimination of potential safety hazards and participation in activities which promotes recycling, replacement, and reduction of resource materials.
- Safety & health accountability: Safety and health are important to BD, and we encourage the observance of all safety programs and training assigned to you. Such programs are to be attended in a timely manner to ensure that work tasks carried out are in accordance with our safety guidelines and SOPs.
- Good Manufacturing Practice (GMP) accountability. Observing GMP rules and procedures.
- Observe BD Code of Ethics
- Reporting up on all incidents / accidents, near misses, deviations from plan and when required, to take part in further investigations.
- Reporting up on all quality incidents, near misses, non-conformance from SOP, Specifications and when required, to take part in further investigations.

B. Operation Tasks
- Lead a team of QA auditors to perform incoming QA inspection.
- Perform investigation and ensure effective containment on raw material for nonconformance reported.
- Review investigation report from supplier to ensure its completeness and effectiveness.
- Handle the non-conforming material per non-conformance product handling procedure.
- Oversee the non-conforming containment activities, with proper segregation.
- Raise QN, block affected parts and release incoming materials/components that is meeting the acceptance criteria timely.
- Feedback incoming materials/product discrepancy to vendor and liaise with material release.
- Participate in project undertaken by the team. E.g., Data collection on quality improvement project.
- Perform visual inspection, dimensional inspection, and documentation verification for incoming received materials audit.
- Update database with inspection result and generate weekly / monthly quality inspection trend report.
- Ensure proper maintenance and retention of inspection quality records and support for retrieval.

C. Supporting Tasks
- Contribute into departments activities that are needed in order to achieve goals set for the department eg. Kaizen submission, team building, safety kaizen submission, and others.
- Participate in the discussion and review of team's performance in the daily shift changeover meeting.
- Participate in continuous improvement initiative / activities.
- Perform any other tasks as assigned.

Preferred Requirements

Education and Experience
- Higher Nitec with at least 5 years relevant QA experience in medical device industry.
- Diploma in Engineering with at least 2 years relevant QA experience in any manufacturing industry.
- Minimum 2 years of related working experience in QA function.

Knowledge and Skills
- Able to read, write, and speak in English.
- Understand the methodology of root cause analysis, nonconformance investigation.
- Supervisory skill is a bonus.

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:
Primary Work Location

SGP Tuas - Tuas Plant

Additional Locations

Work Shift

SG Normal Production (Singapore)