MedTech Supplier Quality Engineer - Impact & Compliance

Becton Dickinson; Canaan (CT); On-site; USD 70,000 - 95,000; Full time

Job summary

Becton Dickinson is hiring a Supplier Quality Engineer in Connecticut to lead incoming material quality, supplier audits, and continuous improvement across BD's supplier base. You will partner with production, engineering and materials teams to ensure compliant, high-quality materials for manufacturing.

The role requires a B.S./B.A. in a science-related field and at least 1 year of supplier quality experience, with preference for ISO 13485:2016 exposure and medical device experience.

Qualifications

• B.S./B.A. in science, QA, engineering or math related field.
• Minimum 1 year supplier quality experience.
• Familiarity with ISO 13485:2016 and medical devices preferred.

Responsibilities

• Perform incoming raw material inspections and approve material releases.
• Collaborate with Production, Material Control, Engineering and cross-functional teams to meet supplier quality requirements.
• Act as a quality and regulatory resource for plant operations and external stakeholders.
• Investigate and resolve incoming material quality issues.
• Coordinate disposition of nonconforming materials with Material Control and suppliers.
• Lead supplier audits and support supplier assessments and evaluations.
• Maintain Approved Supplier Lists (ASL) and supplier documentation.
• Support regulatory, customer, and internal audits (FDA, NSAI, MDSAP).
• Drive continuous improvement initiatives using quality methodologies.

Skills

Supplier quality experience

Validations IQOQPQ

Continuous improvement

Education

Science/Engineering degree

Job description

Becton Dickinson is hiring a Supplier Quality Engineer in Connecticut to lead incoming material quality, supplier audits, and continuous improvement across BD's supplier base. You will partner with production, engineering and materials teams to ensure compliant, high-quality materials for manufacturing.

The role requires a B.S./B.A. in a science-related field and at least 1 year of supplier quality experience, with preference for ISO 13485:2016 exposure and medical device experience.