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Manufacturing Quality Engineer
Manufacturing Quality Engineer-March 2024
Columbus
Mar 28, 2026
About Manufacturing Quality Engineer

  Job Description Summary

  GENERAL FUNCTION:

  To assist the Manufacturing Departments in the establishment and implementation of programs designed to assure control of processes and products toward established standards of quality.

  To use problem solving techniques to increase quality and productivity within the business.

  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.

  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.

  JG 3

  PCP Level- NA

  Responsibility:

  Crucial responsibilities include but are not limited to:

  Develop, change, and supervise in-process inspections to ensure the greatest value in process control for the customer and the plant during the manufacturing process while meeting regulatory requirements.

  Process monitoring and adjustment, process and product improvement, including corrective action plans to address complaint issues.

  Documentation of these activities along with the review and maintenance of S.O., O.I.s and department specific operating procedures such as manufacturing cleaning procedures.

  Employee training of Quality Control concerns regarding Process specifications.

  Develop and implement procedures applicable to the total plant manufacturing process.

  Coordinate efforts with Process Engineering, Production for the establishment of controls, which support current product designs, and process capabilities for assigned product lines. Assistance in such areas as process validation, process acceptance, certain audit correction actions, Change Control issuance for process changes.

  Support CAPAs as owner or as part of the support team.

  Monitor the performance of assigned product lines about product quality levels, waste, and rejection rates.

  Leading / mentoring / conducting quality improvement projects thru CI initiatives.

  May acquire Green/Black Belt Certification.

  Assist in the acceptance and validation of process / equipment.

  Review and develop changes in existing or proposed processes or requirements to achieve optimum performance and quality, cost.

  Assume a role of leadership in analyzing and resolving issues, which prevent desired quality levels achievement.

  Develop programs for the maintenance, replacement, and improvement of inspection gauging.

  Stay informed as to the latest requirements of federal regulations and corporate policies regarding medical devices.

  Lead and ensure regulatory compliance is met and that the manufacturing unit is trained on all requirements.

  Own and continue to improve department training systems.

  Monitor customer complaints and trends. Respond as needed for specific corrective action and customer interface.

  Provide support and guidance on quality/ process improvements.

  Ensure that all company safety rules and regulations are followed and promote general plant safety.

  Own and lead efforts to reduce and eliminate rejections.

  Assist in internal/ external audits and supplier certification processes as needed.

  Other duties, as assigned

  Indirect supervision

  Supervision of QC Representatives & other support personnel necessary for assigned project completion.EDUCATION

  Required: Bachelor of Science degree.Experience

  Required: 3 years manufacturing experience with broad background in manufacturing processes

  2 years Process Control experience

  2 years Quality manufacturing experience

  Proven history of product / process improvements utilizing Green/ Black Belt/Six Sigma techniques.

  Ability to generate validation protocols, which align with the globalization standardization initiative.

  Experience working with high performing work teams desired

  3 years practical GMP / Medical Device manufacturing experience.

  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.

  At BD, we strive to make healthcare a priority for our associates and their families. We have a variety of plans including a new HSA Basic plan option with Cigna.

  $0 payroll contributions if your salary is below $50,000

  Plan covers 100% preventative care (annual wellness exam, and immunizations)

  Visit any provider

  If you meet the eligibility and enrollment requirements, your coverage begins on your date of hire or the date you become a benefits-eligible associate.

  BENEFITS:

  BD provides comprehensive total rewards benefits for all of its employees. Most benefits start on day 1 of your employment with BD.

  Competitive pay

  Up to 6 weeks of paid parental leave

  Medical, dental, and vision insurance plans

  Education assistance ($5250.00 per year)

  Adoption assistance

  401K plan with $.75 of every dollar matched up to 6% of compensation

  Basic life and AD&D provided

  Discounted home, auto, and pet insurance plans

  Paid holidays and vacation (pro-rated the first year based on actual start date)

  Excited to grow your career?

  We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!

  Our people make all the difference in our success.

  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/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.

  PDN

  Primary Work Location

  USA NE - Columbus (West)

  Additional Locations

  Work Shift

  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.

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