BD (Becton, Dickinson and Company)-posted about 2 months ago
Full-time • Mid Level
Onsite • Columbus, NE
5,001-10,000 employees
Miscellaneous Manufacturing

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. Job Position Title: Manufacturing Quality Engineer Function: Quality Location: Columbus West Job Group/Grade: JG3 Position Summary: Assist the Manufacturing Departments in the establishment and implementation of programs designed to assure control of processes and products toward established standards of quality. Use problem solving techniques to increase quality and productivity within the business. Validate new products, processes, equipment. Ensures compliance with BD quality systems, policies, procedures and best practices, and all local, state, federal and BD safety regulations, policies and procedures. Regular, punctual attendance is an essential job function. Ability to write programs supporting the implementation of the eDHR project. Ability to read and write and converse in English. Willing and able to uphold BD Values.

  • 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. Create validation documentation for new products, processes, equipment
  • Coordinate efforts with Process Engineering, Production, and Projects 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 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 required to support the needs of the business
  • Bachelor's degree required
  • Three years manufacturing experience with broad background in manufacturing process
  • Two years Process Control experience
  • Three years practical GMP/Medical Device manufacturing experience
  • Effective Oral/written Communication - Proficient
  • Ability to work as part of a team / Teambuilding - Advanced
  • Independent thinking / Self Driven - Proficient
  • Decision Making Ability - Proficient
  • Computer Skills / Microsoft Office - Proficient
  • eDHR related software.
  • Product / process improvements utilizing Green/ Black Belt/Six Sigma techniques.
  • Ability to generate validation protocols, which align with the globalization standardization initiative.
  • Experience in validations, new products, processes and materials, preferred.
  • Competitive pay
  • Access a portion of your pay before pay day with DailyPay
  • Healthcare coverage: No paycheck contributions for eligible associates under a certain salary threshold enrolled in the HSA Basic Medical Plan option, no matter how many dependents you cover.
  • Preventive care covered at 100%.
  • Dental and vision insurance at group rates.
  • Paid parental leave up to 6 weeks
  • Adoption assistance plan
  • 401(k) plan with 75 cents on the dollar matched by BD up to 6% of compensation
  • Company paid basic life and AD&D insurance
  • Tuition reimbursement
  • Discounted home, auto and pet insurance
  • Paid holidays and vacation (pro-rated the first year based on actual start date)
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service