About the role
Job Description
Job Description
- Summary The Quality Engineer II will assist the Manufacturing Departments in the establishment and implementation of programs designed to assure control of processes and products toward established quality standards. Use problem solving techniques to improve quality within the business. Justification Addition Responsibilities may include but are not limited to
- Ensure that all company safety rules and regulations are followed and promote general plant safety.
- Work with Process Engineering to implement plant driven changes and provide overall support of process improvements by working with engineering teams to implement process improvements to improve Quality, conducting quality improvement projects through various CI initiatives.
- Develop or update in-process inspection requirements to ensure the greatest value in process control for the customer and the plant during the manufacturing process while meeting regulatory requirements.
- Provide assistance in such areas as process/equipment validation, process and product acceptance, audit correction actions, Change Control issuance for process changes.
- Support CAPAs as owner or as part of the support team Monitor the performance of product lines for product quality metrics.
- Work to implement document changes in support of ongoing efforts to simplify internal quality procedures in alignment with business unit and corporate requirements. Leading investigations for quality issues resulting in large rejections by using applicable problem solving and root cause techniques. Complete training in order to support Manufacturing Quality for day-to-day operations including assuring product release, manufacturing quality training and defect containment. This also includes support of the 24/7 operation for manufacturing Quality. One week a month rotation. On call one week a month. Other duties, as assigned. Education Bachelor's degree is required.
- Experience Required 3 years manufacturing experience with broad background in manufacturing processes. Desired 3 years practical GMP / Medical Device manufacturing experience. 2 years Quality manufacturing experience
- Strong interpersonal skills with ability to work in a team environment. Why Join Us? 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 healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. 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. Required Skills Optional Skills . Primary Work Location USA CT - Canaan Additional Locations Work Shift NA (United States of America)