Quality Engineer I: Risk & Process Control

Abbott Laboratories; Roseville (MN); On-site; USD 51,000 - 101,000; Full time

Benefits offered by this job

Free medical coverage (HIP PPO)

Retirement plan with high employer +

Tuition reimbursement

Education benefit (FreeU)

Global employer recognized as great to

Job summary

Abbott in Minnesota is seeking a Quality Engineer I to advance quality engineering methodologies across new product development, manufacturing, and support. The role features a rotation starting in risk management and patient safety, then moving into operations quality, with emphasis on process controls and CAPA systems.

You'll apply data analysis, problem-solving, and cross-functional collaboration to identify and resolve quality issues in a fast-paced, matrixed environment.

Qualifications

• Bachelor’s Degree in Engineering or technical field.
• 2+ years of engineering experience.
• Knowledge of quality tools and methodologies.
• Strong communication and interpersonal skills.
• Ability to work in a matrixed and diverse environment.
• Multitask and meet deadlines in a fast-paced setting.

Responsibilities

• Identify, review, and implement process controls for development, qualification, and manufacturing.
• Perform risk assessments including FMEA, change management, and investigation/resolution.
• Lead assurances, process controls, and CAPA systems to meet requirements.
• Assist in developing streamlined business systems to identify and resolve quality issues.
• Apply systematic problem-solving to prioritize and resolve quality issues.
• Document experiment plans, results, protocols, and reports.
• Lead CTQ parameter monitoring and investigations of non-conformances.
• Participate in cross-functional teams as a Core Team Member.

Skills

Quality tools

Statistical analysis

Data analysis

Cross-functional collaboration

Communication skills

Problem solving

Education

Bachelor's Degree in Engineering or Technical Field

Job description

Abbott in Minnesota is seeking a Quality Engineer I to advance quality engineering methodologies across new product development, manufacturing, and support. The role features a rotation starting in risk management and patient safety, then moving into operations quality, with emphasis on process controls and CAPA systems.

You'll apply data analysis, problem-solving, and cross-functional collaboration to identify and resolve quality issues in a fast-paced, matrixed environment.