Abbott

Healthcare

QualityEngineerI

$51–101k Liberty, South Carolina, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Quality Engineer I at Abbott. Skills: Quality engineering, Process control, Problem-solving, Risk analysis. Identify process control systems. Implement process control systems”

Industry & Context.

Healthcare
Problems you'll solve

Problem-solving methodologies; Root cause analysis; Data-driven decision making

Eligibility Requirements

5% travel, Continuous sitting, Keyboard use

What They're Looking For.

Must Have

BS degree in Engineering or Technical Field, 0-2 years of experience, 2 years of Engineering experience, Demonstrated use of Quality tools/methodologies, Detailed knowledge of FDA, Detailed knowledge of GMP, Detailed knowledge of ISO 13485, Detailed knowledge of ISO 14971, Solid communication skills, Solid interpersonal skills, Project management skills, Leadership skills, Ability to lead multi-departmental project teams, Ability to resolve quality issues, Advanced computer skills, Statistical/data analysis skills, Report writing skills, Ability to work in a highly matrixed environment, Ability to work in a geographically diverse environment, Ability to work within a team, Ability to work as an individual contributor, Ability to work in a fast-paced environment, Ability to work in a changing environment, Ability to leverage others for projects, Ability to engage others for projects, Verbal communications, Written communications, Ability to communicate at multiple levels, Multitasks, Prioritizes, Meets deadlines, Organizational skills, Follow-up skills, Attention to detail

Nice to Have

Masters Degree preferred, Prior medical device experience preferred, Experience implementing Six Sigma, Experience implementing Lean Manufacturing, ASQ CQE certification preferred, Other certifications preferred, Experience working in a broader enterprise model preferred, Experience working in a cross-division business unit model preferred

What You'll Do.

Identify process control systems

Implement process control systems

Lead assurance implementation

Lead process control implementation

Lead CAPA systems implementation

Assist in business systems development

Assist in business systems execution

Apply problem-solving methodologies

Identify quality issues

Prioritize quality issues

Communicate quality issues

Resolve quality issues

Document experiment plans

Document experiment results

Lead CTQ parameter control

Lead CTQ parameter monitoring

Lead product improvement methodologies

Lead process improvement methodologies

Lead non-conformance investigation

Lead non-conformance resolution

Lead non-conformance prevention

Participate in quality teams

Represent Quality function

Complete risk analysis

Maintain risk analysis

Work with design engineering

Work with microbiology

Ensure environmental monitoring

Consider microbiology requirements

Support Company initiatives

Support Quality Management Systems

Support Environmental Management Systems

Support regulatory requirements

Comply with FDA regulations

Comply with other regulatory requirements

Comply with Company policies

Comply with operating procedures

Maintain positive communications

Maintain cooperative communications

Perform related duties

How You'll Work.

Team & Collaboration

Core Team Member; Multi-departmental project teams; Cross-functional teams

Communication Scope

Verbal communications; Written communications; Communicate at multiple levels

Process & Methodology

Project management, Leadership

Full Job Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. ## **JOB DESCRIPTION:** A healthy heart is essential to good health. That's why we're committed to advancing treatments for people with cardiovascular disease. As a global leader in Cardiac Rhythm Technologies, our breakthrough medical technologies help restore people's health so they can get back to living their best lives, faster. We focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. We are seeking an experienced, high caliber **_Quality Engineer I_** for our **_Liberty, South Carolina_** location. This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. **WHAT YOU’LL DO** \- Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements \- Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements \- Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues \- Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues \- Design and conduct experiments for process optimization and/or improvement -Appropriately document experiment plans and results, including protocol writing and reports \- Lead process control and monitoring of CTQ parameters and specific

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