of our billions of Med Tech 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. Are you a dynamic and experienced Quality Manager? Do you have a passion for improving processes and reducing waste? If so, we want you to join our team as our new Quality Manager! In this role, you will be responsible for coordinating the activities of the quality assurance function within your business
unit, informing all inspection and management personnel of quality problems and solutions. You will evaluate all changes, modifications and additions to product lines and determine the effect on product quality and costs.
You will provide resources for quality improvement activities, including waste reduction, cost reduction and process validation. You will report directly to the Associate Director, Quality. Responsibilities Provides leadership and supervision (either directly or indirectly) for all salaried and hourly associates assigned to the responsible business unit. Hire, train, coach, and motivate associates to drive the company attainment and business unit quality objectives.
Responsible for the performance management process and development. Plan and conduct product and process verification and testing activities within the business unit value stream, including the assignment of resources.
Report and attain key quality and business metrics within the assigned business unit. Initiate capability studies of processes to identify causes of chronic levels of defects and remedy those areas associated with a high cost of quality. Review inspection systems, methods and procedures for optimization of quality and resources. Recommend and explain capital expenditures and validate to implementation. Provides functional support to the Engineering Department for the writing of protocols, data gathering and data analysis associated with the Plant Validation Program - including prospective, retrospective and revalidation efforts.
Conduct process capability studies and/or process optimization studies prior to validations. Takes lead in Process Characterization activities within the assigned business unit. Acquires data from critical processes allowing for trend analysis and recommends action to be taken to maintain/acquire statistical process control. Communicates and coordinates with required organizations in FLKS to drive resolution of quality activities (SAs, ACRs, Validations, NCMRs, Variances, Escalated Customer Complaints, C2W, etc.
)Assure coordination of the overall quality effort within the business unit in the following areas: Provide plant self-audit information on the product and process to assure compliance with all government regulations (QSR, FDA, and Contractual). Periodically review Quality specifications to assure accuracy and adequacy. Formulate and implement policies and procedures relating to product quality or process control as appropriate. Provide test and statistical support for customer complaint issues that arise and make recommendations on actions to be taken.
Support Metrology activities and Gauge calibration program. Additional Responsibilities: Operates within the Safety and QSR guidelines of BD-Sumter. Performs miscellaneous duties as required by management. Requirements: Requires a minimum of a BS degree in science, engineering, or relevant field. Engineering Major is preferred Minimum of 3 years quality assurance experience3 years of quality management/leadership experience Strong management, team skills, and influential management highly desired Able to communicate precisely and accurately to all levels of the organization.
ASQ certifications CQE, CSQE, CRE, CMQ/OE, CSSGB and/or CSSBB highly desired. Proven understanding of QSRs and/or ISO13485 and/or FDA preferred Six Sigma training (Preferred)Experience in the Medical Device area would be an advantage. If you're a highly motivated individual with a passion for quality, we want you on our team. Apply now and join us as our new Quality Manager! 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 /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
PDN Primary Work Location USA SC - Sumter Additional Locations Work Shift Apply Save Job Responsibilities Job Description Summary 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 Med Tech 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. Are you a dynamic and experienced Quality Manager? Do you have a passion for improving processes and reducing waste? If so, we want you to join our team as our new Quality Manager! In this role, you will be responsible for coordinating the activities of the quality assurance function within your business unit, informing all inspection and management personnel of quality problems and solutions.
You will evaluate all changes, modifications and additions to product lines and determine the effect on product quality and costs. You will provide resources for quality improvement activities, including waste reduction, cost reduction and process validation. You will report directly to the Associate Director, Quality. Responsibilities Provides leadership and supervision (either directly or indirectly) for all salaried and hourly associates assigned to the responsible business unit.
Hire, train, coach, and motivate associates to drive the company attainment and business unit quality objectives. Responsible for the performance management process and development. Plan and conduct product and process verification and testing activities within the business unit value stream, including the assignment of resources. Report and attain key quality and business metrics within the assigned business unit. Initiate capability studies of processes to identify causes of chronic levels of defects and remedy those areas associated with a high cost of quality.
Review inspection systems, methods and procedures for optimization of quality and resources. Recommend and explain capital expenditures and validate to implementation. Provides functional support to the Engineering Department for the writing of protocols, data gathering and data analysis associated with the Plant Validation Program - including prospective, retrospective and revalidation efforts. Conduct process capability studies and/or process optimization studies prior to validations. Takes lead in Process Characterization activities within the assigned business unit.
Acquires data from critical processes allowing for trend analysis and recommends action to be taken to maintain/acquire statistical process control. Communicates and coordinates with required organizations in FLKS to drive resolution of quality activities (SAs, ACRs, Validations, NCMRs, Variances, Escalated Customer Complaints, C2W, etc. )Assure coordination of the overall quality effort within the business unit in the following areas: Provide plant self-audit information on the product and process to assure compliance with all government regulations (QSR, FDA, and Contractual). Periodically review Quality specifications to assure accuracy and adequacy.
Formulate and implement policies and procedures relating to product quality or process control as appropriate. Provide test and statistical support for customer complaint issues that arise and make recommendations on actions to be taken. Support Metrology activities and Gauge calibration program. Additional Responsibilities: Operates within the Safety and QSR guidelines of BD-Sumter. Performs miscellaneous duties as required by management. Requirements: Requires a minimum of a BS degree in science, engineering, or relevant field.
Engineering Major is preferred Minimum of 3 years quality assurance experience3 years of quality management/leadership experience Strong management, team skills, and influential management highly desired Able to communicate precisely and accurately to all levels of the organization. ASQ certifications CQE, CSQE, CRE, CMQ/OE, CSSGB and/or CSSBB highly desired. Proven understanding of QSRs and/or ISO13485 and/or FDA preferred Six Sigma training (Preferred)Experience in the Medical Device area would be an advantage. If you're a highly motivated individual with a passion for quality, we want you on our team.
Apply now and join us as our new Quality Manager! 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 /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer.
We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. PDN Primary Work Location USA SC - Sumter Additional Locations Work Shift Apply Save Job PDN-9a5500d1-7b62-474f-93bc-10953dbd0d21
