Quality Engineer

Quality Engineer

BH Job ID:


4575

SF Job Req ID:


19145

Ingersoll Rand is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical
care leave, gender identity or expression, genetic information, marital status, medical
condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.

Job title:

Quality Engineer

Location:
Lincolnshire, IL

About Us


Imagine a company with technology leadership of over 160 years, yet it operates with the energy of a startup. Ingersoll Rand has dedicated itself to Making Life Better for its employees, customers, shareholders, and planets. We produce innovative and mission-critical flow creation and life science technologies - from compressors
to precision handling of liquids, gasses, and powers - to increase industrial productivity, efficiency, and sustainability. Supported by over 80+ brands, our products are used in various end-markets including life sciences, food and beverage, clean energy, industrial manufacturing
, infrastructure, and more. Across the globe, we're driving growth with an entrepreneurial spirit and ownership mindset. Learn more at irco.com and join us to own your future.

Job Overview:


The Quality Engineer
( QE
) ensures that products, manufacturing
processes, and Quality Management System
( QMS
) activities meet established quality standards and regulatory requirements. This role combines technical quality engineering with ownership of key QMS
processes, including document control, training, record management, and audit readiness. The QE
works cross-functionally with Engineering, Manufacturing
, and other teams to support New Product Introduction
( NPI
) and sustaining operations, ensuring timely execution of validation
, risk management, and quality deliverables. The role is also responsible for investigating and resolving nonconformances through CAPA, driving continuous improvement
, and supporting the effectiveness of the electronic QMS
(e.g., MasterControl
) to ensure data integrity and efficient processes.

Responsibilities:

• Own and maintain the Quality Management System
  ( QMS
  ), including document control, change management, quality records, electronic QMS
  (e.g., MasterControl
  ), and training, ensuring compliance with FDA
  , ISO, and internal requirements.
  
  
  
• Review and approve change controls; oversee calibration and equipment control programs; and drive continuous improvement
  of QMS
  processes and systems.

• Support New Product Introduction
  ( NPI
  ) by ensuring compliance with validation
  ( IQ
  / OQ
  / PQ
  ), risk management, statistical analysis, customer specifications, and regulatory requirements.

• Partner with Engineering to support sustaining manufacturing
  , change control, equipment maintenance, revalidation, and process improvement initiatives.

• Perform Device History Record
  ( DHR
  ) reviews; lead or support investigations for nonconformances and CAPAs; and drive root cause analysis
  , corrective actions, and right-first-time improvements.

• Lead risk management activities, including risk assessments and pFMEA
  , and ensure effective mitigation strategies.

• Lead and support internal, customer, ISO, and FDA
  audits; represent Quality in customer and supplier interactions; and support supplier qualification and performance monitoring.

• Support cross-functional and cross-site quality initiatives, special projects, and foster a culture of quality, compliance, continuous improvement
  , and proactive risk management.

Requirements

• Bachelor's degree (BA/BS) in Engineering, Quality, Life Sciences, or a related technical field
  
  
  
• 1+ years of experience in Quality Engineering, Quality Systems, or a similar role within a medical device
  or regulated manufacturing
  environment

Preference:

• Working knowledge of Quality Management Systems ( QMS
  ), including document control, training systems, record retention, and audit support
  
  
  
• Familiarity with FDA 21 CFR Part 820
  and ISO 13485
  requirements

• Experience with electronic Quality Management Systems
  ( eQMS
  ) such as MasterControl
  or similar preferred

• Strong technical writing and documentation skills, including development and revision of SOPs, work instructions, validation
  documents, and quality records

• Proficiency in Microsoft Office (Excel, Word, PowerPoint)

• Lead Auditor Certification is an advantage

Travel & Work Arrangements/Requirements

• Fully site based, flexible working, hybrid, 50% travel across Europe, etc)
  
  
  

Pay Range:


The pay range for this role is $65,000-$80,000. The pay range considers a wide range of factors that include a candidate's skills; experience and training; licensure and certifications; and geographic location.

What we Offer


At Ingersoll Rand, we embrace a culture of personal ownership - taking responsibility for our company, our communities, and our environment, as well as our individual health and well-being. Our comprehensive benefits package is designed to empower you with the tools and support necessary to take charge of your health, ensuring that together, we can continue to make life better. Our range of benefits includes health care options like medical
and prescription plans, dental and vision coverage, as well as wellness programs. Additionally, we provide life insurance, a robust 401(k) plan, paid time off, and even an employee stock grant, among other offerings. These benefits are our commitment to you, so you can be your best at work and beyond.

Ingersoll Rand Inc. (NYSE:IR), driven by an entrepreneurial spirit and ownership mindset, is dedicated to helping make life better for our employees, customers and communities. Customers lean
on us for our technology-driven excellence in mission-critical flow creation and industrial solutions across 40+ respected brands where our products and services excel in the most complex and harsh conditions. Our employees develop customers for life through their daily commitment to expertise, productivity and efficiency. For more information, visit

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