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 Description Summary:
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. 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. Develop programs for the maintenance, replacement, and improvement of inspection gauging. 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.
Qualifications:
Master’s degree in Engineering (any) or related field of study and one (1) year of experience in the job offered or related occupation in which the required experience was gained. In lieu of a Master’s degree in Engineering (any) or related field of study and one (1) year of experience, the employer will also accept a Bachelor’s degree in Engineering (any) or related field of study and one (1) year of experience in the job offered or related occupation in which the required experience was gained. Must have demonstrated experience with: Validation of new processes and new equipment; Change Control owner and implementation; Documentation per Regulatory Requirements; External and internal Audit; Statistical analysis; 21 CFR Part 820 Quality Systems Regulations - FDA regulations and requirements as it pertains to medical devices; ISO-9001 Quality Systems Standards - regulations and requirements as it pertains to Quality Systems for a medical device company; Six Sigma- Tools for Quality investigations and process improvements including: demonstration of a rigorous performance improvement approach; customer focus, data driven approach to understand process variation and process capabilities; and utilization of DMAIC tools.
Primary Work Location:
1852 10th Ave., Columbus, NE 68601
Additional Locations:
N/A
Work Shift:
Not Specified
To apply, mail resume to Becton, Dickinson and Company, Attn: BDHR – DT, 3750 Torrey View Ct, San Diego, CA 92130, OR submit a resume to https://neworks.nebraska.gov/vosnet/Default.aspx, OR submit a resume to https://bdx.wd1.myworkdayjobs.com/EXTERNAL_CAREER_SITE_USA. Must reference Job Title & Job Code: R-521726. EOE.
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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 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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USA NE - Columbus (West)