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:
Sr Quality Engineer
Location:
Salt Lake City, UT
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 Senior Quality Engineer is responsible for ensuring compliance with Quality Management System (QMS) and applicable regulatory requirements within our medical device manufacturing
environment. This role encompasses a wide range of responsibilities, including validation activities, process improvements, nonconformance and CAPA management, auditing responsibilities, risk assessments, and training initiatives. The Senior Quality Engineer also collaborates across departments to enhance current manufacturing
/quality processes and supports new product introductions. The Senior Quality Engineer is expected to provide guidance and leadership to other members of the quality department, including Document Technicians, Quality Inspectors, and Quality Engineers.
Responsibilities:
- Co-manage the New Product Introduction (NPI) and sustaining manufacturing processes by ensuring compliance with required documentation, validations, customer specifications, ISO standards, and regulatory requirements.
- Review, approve, and manage engineering and change-control documentation, including validation protocols/reports, manufacturing procedures, sample requests, and customer change submissions through completion.
- Develop, maintain, and improve procedures, work instructions, and QMS documentation in compliance with FDA regulations, ISO standards, and applicable environmental and cleanroom requirements.
- Lead risk management, nonconformance resolution, and CAPA activities, including root cause analysis, pFMEAs, complaint investigations, and corrective/preventive action implementation.
- Monitor, analyze, and report key quality metrics, providing regular updates to management and driving continuous improvement initiatives.
- Support and lead customer, supplier, ISO, and FDA audits and inspections, ensuring audit readiness and effective representation of Flexan.
- Contribute to the Supplier Management Program, including supplier assessments, approved supplier list maintenance, customer surveys, and supplier/customer engagement.
- Promote a strong culture of quality by collaborating cross-functionally, delivering employee training, supporting the Quality Manager, and serving as a backup for key quality functions as needed.
Requirements:
- BA / BS in Engineering or related field.
- 5+ years of Quality Engineering or similar experience in a medical device manufacturing environment and/or regulated industry.
Preferences:
- Robust knowledge of Failure Mode Effects Analysis (FMEA) and Production Part Approval Process (PPAP)
- Strong technical writing skills
- Experience with supplier quality functions, including management of approved vendor lists
- Demonstrated experience in process improvement methodologies.
- Active involvement in FDA and ISO audits, with a strong understanding of regulatory compliance requirements.
- Detailed knowledge of FDA 21 CFR 820, ISO 13485, and ISO 14644-1.
- Strong analytical skills with emphasis on statistical/data analysis
- Ability to coach and develop others
- Ability to drive/lead in a matrix structure with persuasion and influence
- Organization and time management skills are essential
- Creativity, verbal and written communication skills, and problem-solving ability
- Team player that gets along well with others (respectful of supervisors and co-workers, helps others by offering ideas when appropriate)
- Follows through on tasks and projects as assigned
Core Competencies:
- Quality
- Accountability
- Respect
- Innovation
- Integrity
- Open & honest communications
- Teamwork
- Customer focus
Travel & Work Arrangements/Requirements:
Onsite
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 www.IRCO.com.
To Apply:
Please apply via our website https://ir-jobs.dzconnex.com/
by February 2026 in order to be considered for this position.
