Quality Engineer: MedTech Validation & Process Improvement

Becton, Dickinson and Company (BD); United States; On-site; USD 84,000 - 134,000; Full time

Benefits offered by this job

Annual Bonus

Discretionary LTI Bonus

Medical coverage

Health Savings Accounts

Job summary

Becton, Dickinson and Company (BD) is seeking a Quality Engineer at its Delran, USA site to author, review and approve QMS documents. You will participate in project teams, investigate quality issues, and drive CAPAs to improve processes and meet regulatory standards.

The role requires a Bachelor's in Biomedical/Engineering or related field and 3 years in medical devices or manufacturing in a quality engineering capacity. On-site work with strong collaboration across teams is expected.

Qualifications

• Bachelor’s degree in Biomedical/Engineering or related field.
• 3 years of experience in medical devices/manufacturing in a Quality Engineering role or equivalent.

Responsibilities

• Lead validation activities and author/execute protocols for new product development and process changes.
• Provide technical and quality engineering support for manufacturing and sustaining projects.
• Investigate quality issues, initiate NCRs, and manage MRB processes; drive CAPAs.

Skills

Quality engineering

Regulatory knowledge

Statistical analysis

Documentation

Communication

Education

Bachelor’s Degree in Biomedical/Engineering or related field

Tools

Minitab

MS Excel

Job description

Becton, Dickinson and Company (BD) is seeking a Quality Engineer at its Delran, USA site to author, review and approve QMS documents. You will participate in project teams, investigate quality issues, and drive CAPAs to improve processes and meet regulatory standards.

The role requires a Bachelor's in Biomedical/Engineering or related field and 3 years in medical devices or manufacturing in a quality engineering capacity. On-site work with strong collaboration across teams is expected.