MedTech Quality Engineer: CAPA, Validation & Data-Driven Impact

BD; Columbus (OH); On-site; USD 70,000 - 90,000; Full time

Job summary

BD is seeking a Quality Engineer at its USA Columbus location to oversee quality for a product line across multiple processes. You will participate in audits, drive root-cause investigations and CAPA, and support validations to ensure product quality and cost targets.

A BA/BS in engineering and 0–5 years’ experience in a quality/technical role are preferred. Experience in Pharma, Biotech or Medical Device manufacturing is a plus.

Qualifications

• Minimum BA/BS in Engineering in a technical field.
• 0–5 years’ experience in a quality/technical role.
• Experience at Pharma, Biotech or Medical Device manufacturer preferred.

Responsibilities

• Oversees Quality needs for a product line across multiple processes.
• Assist and/or manage plant projects and drive to completion.
• Participate in audits as process and quality systems.
• Develop Root cause investigation and CAPA experience.
• Develop understanding of the validation system and assist in validations.
• Conduct Measurement System Analysis.
• Conduct diagnostic and statistical analysis to improve quality, reliability and cost.
• Assist in meeting plant team plans for cost and quality improvement, operating within department budget guidelines.
• Make data-driven decisions and complete investigations and validations.
• Completion of projects on time and on budget.

Skills

Problem solving

Project management

Data driven

Statistical

Communication

Education

BA/BS in Engineering (Applied, Automotive, Computer/Information, Electrical, Electronic, Industrial, Manufacturing, Mechatronic, Process or Project Engineering)

Job description

BD is seeking a Quality Engineer at its USA Columbus location to oversee quality for a product line across multiple processes. You will participate in audits, drive root-cause investigations and CAPA, and support validations to ensure product quality and cost targets.

A BA/BS in engineering and 0–5 years’ experience in a quality/technical role are preferred. Experience in Pharma, Biotech or Medical Device manufacturing is a plus.