Supplier Quality Engineer

BD (Becton, Dickinson and Company) • Zelienople, PA

52d • Onsite

About The Position

The Supplier Quality Engineer is responsible for the application and interpretation of the plant/department procedures to ensure consistency and compliance with Quality Systems. The Senior Quality Engineer uses the Company Quality Systems to ensure overall compliance and has the knowledge necessary to apply the appropriate statistical and analytical tools to ensure the parts and materials used to manufacture medical devices meet requirements and specifications. 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. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Typical assignments may include: Partnering with Plant suppliers to resolve and prevent technical issues. Guidance on supplier-related projects relative to products, policies and continuous improvement. Review procedures for compliance to FDA, Corporate and International standards. Analyze data to proactively identify emerging and systemic production, measurement or design issues. Investigate product issues in the form of Quality Notifications and Customer Complaints, and leads supplier corrective actions. Key contact/liaison with Supplier/OEM quality departments to drive consistency in practices as needed. Responsible for the ASL Material Review Board member - Disposition and resolve non-conformance issues of supplied materials Helps manage supplier performance metrics (scorecards) with the materials group, identifies suppliers who are not meeting required levels, issues Supplier Corrective Action Reports (SCAR) or other performance improvement initiatives and ensures completion as planned At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. 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. 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.

Requirements

• Bachelor's degree in Engineering or related field required. Preferred degree would be in Mechanical, Electrical or Industrial Engineering, Biological Sciences, Chemistry, and/or Computer Science or other related field.
• Applicants must be authorized to work for ANY employer in the US. We are unable to sponsor or take over sponsorship of employment Visa at this time.
• Must demonstrate a working understanding of the pertinent Quality Systems Regulations (i.e.: Good Manufacturing Practices, ISO, FDA).
• Proven track record to develop solutions to a variety of problems of moderate scope and complexity, using policies and procedures for guidance.
• Capable of using Microsoft programs and ability to learn other systems.
• Working knowledge of statistical methods as well as statistical application software.
• Effective verbal and written communication skills.
• The ability to work in teams and independently with minimal supervision to obtain results as required.
• Must be self-motivated/directed, organized, detail oriented and have ability to multi-task projects.

Nice To Haves

• Preferred: Minimum 1-3 years' experience in a medical device manufacturing environment in a supplier quality function.
• Professional certification is an advantage (i.e. CQA, CQE, SQE, CQM, Six Sigma, etc.).

Responsibilities

• Partnering with Plant suppliers to resolve and prevent technical issues.
• Guidance on supplier-related projects relative to products, policies and continuous improvement.
• Review procedures for compliance to FDA, Corporate and International standards.
• Analyze data to proactively identify emerging and systemic production, measurement or design issues.
• Investigate product issues in the form of Quality Notifications and Customer Complaints, and leads supplier corrective actions.
• Key contact/liaison with Supplier/OEM quality departments to drive consistency in practices as needed.
• Responsible for the ASL
• Material Review Board member - Disposition and resolve non-conformance issues of supplied materials
• Helps manage supplier performance metrics (scorecards) with the materials group, identifies suppliers who are not meeting required levels, issues Supplier Corrective Action Reports (SCAR) or other performance improvement initiatives and ensures completion as planned

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Miscellaneous Manufacturing
• Number of Employees: 5,001-10,000 employees