About this opportunity
Becton Dickinson lists this Quality Engineer opportunity in riverside park, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Becton Dickinson seeks a Quality Engineer for its Delran, New Jersey manufacturing facility. The role involves developing quality documentation, leading validation activities, investigating quality issues, and ensuring compliance with regulatory standards for medical device production.
Responsibilities
Author, review, and approve quality management system documents and records
Lead validation activities including protocol development for new products and process improvements
Design and conduct quality studies to identify root causes and drive process improvements
Investigate quality issues, initiate nonconformance reports, and manage Material Review Board processes
Review and approve inspection records, environmental monitoring data, and Lot History Records for compliance
Requirements
Bachelor's degree in Biomedical Engineering or related field
3+ years quality engineering experience in medical devices or manufacturing
Knowledge of FDA QSR and ISO 13485 standards
Proficiency with statistical software such as Minitab and MS Excel
Strong oral and written communication skills
Project planning skills and ability to meet customer needs
#J-18808-Ljbffr
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.