Quality Engineer II

Requirements

• 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?
• 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 .
• Required Skills
• Optional Skills
• .
• Primary Work Location
• USA CT - Canaan
• Additional Locations
• Work Shift
• NA (United States of America)

Benefits

Additional Information

We are the people who give possibilities purpose 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. 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.

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