Abbott

Healthcare

QualityEngineerII

$61–123k Atlanta, Georgia, United States FULL TIME
The Brief

“Quality Engineer II at Abbott. Skills: Quality engineering, Manufacturing support, Continuous improvement, Compliance. Provide quality engineering support for manufacturing operations. Support production activities to ensure compliance”

Industry & Context.

Healthcare
Problems you'll solve

Root cause analysis; Investigation; Analysis

Eligibility Requirements

10 % travel, Continuous sitting, Continuous standing

What They're Looking For.

Must Have

Bachelor's degree in Engineering, Science, or related technical field with 3+ years of quality engineering, manufacturing engineering, or related experience, Master's degree in Engineering, Science, or related technical field with 1+ years of quality engineering, manufacturing engineering, or related experience, Experience in a regulated industry

Nice to Have

Medical device industry experience, ASQ Certified Quality Engineer (CQE) or other ASQ certification, Experience with CAPA, complaints, investigations, audits, and risk management, Knowledge of FDA Quality System Regulation and ISO 13485

What You'll Do.

Provide quality engineering support for manufacturing operations

Support production activities to ensure compliance

Assess manufacturing issues

Recommend corrective actions

Lead investigations associated with complaints

Lead investigations associated with nonconforming material

Lead investigations associated with deviations

Lead investigations associated with quality events

Support CAPA activities

Implement corrective actions

Participate in risk assessments

Participate in quality impact evaluations

Identify opportunities to improve product quality

Identify opportunities to improve process performance

Identify opportunities to improve operational efficiency

Utilize quality engineering tools

Support decision-making

Participate in cross-functional improvement initiatives

Support internal audits

Support external audits

Support regulatory inspections

Ensure compliance with FDA

Ensure compliance with ISO 13485

Ensure compliance with MDR

Ensure compliance with company quality system requirements

Maintain complete quality records

Maintain accurate quality records

Maintain complete quality documentation

Maintain accurate quality documentation

How You'll Work.

Team & Collaboration

Manufacturing; Operations; Engineering; Quality teams; R&D; Regulatory Affairs; Supply Chain

Free ATS check

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