2 weeks ago

Quality Engineer

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 3 hours agoStatus: Live

Job Summary

Ensure products, manufacturing processes, and the Quality Management System (QMS) meet quality and regulatory requirements. Own key QMS processes such as document control, change management, training, and audit readiness, while supporting NPI and sustaining operations. Investigate nonconformances using CAPA and root-cause analysis, lead risk management activities (including pFMEA), and support the electronic QMS effectiveness (MasterControl) to drive data integrity, continuous improvement, and right-first-time performance.

Location: United States

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Own and maintain QMS processes including document control, change management, and quality record retention to ensure FDA/ISO and internal compliance.
•Develop and maintain procedures and work instructions in the electronic QMS (e.g., MasterControl).
•Support NPI and sustaining operations by ensuring validation deliverables (IQ/OQ/PQ), risk management, and regulatory/customer requirements are met.
•Investigate and resolve nonconformances using CAPA, including root cause analysis and effectiveness verification.
•Lead internal and external audits, ensuring audit readiness and timely closure of observations.

Pay and Benefits

Salary: USD 65,000 - 80,000 annually

Equity and Bonus:Equity

Perks:Health InsuranceDentalVision401kPaid LeaveLife InsuranceEquity

Key Requirements

•Bachelor’s degree (BA/BS) in Engineering, Quality, Life Sciences, or a related technical field.
•1–3 years of experience in Quality Engineering, Quality Systems, or a similar role in a medical device or regulated manufacturing environment.
•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 QMS (e.g., MasterControl) and strong technical writing/documentation skills (SOPs, work instructions, validation documents, quality records).

Experience:1-3 yearsMedical deviceRegulated manufacturingLife sciences

Education:Bachelor's

Skills:Technical writingDocumentationContinuous improvementRisk management

Certifications:Lead Auditor Certification

Tech Stack:MasterControlQMSElectronic QMSMicrosoft OfficeExcelWordPowerPoint

Company Brief

Ingersoll Rand

Designs, manufactures, and services industrial equipment and technologies including air compressors, power tools, fluid management systems, and downstream industrial solutions for manufacturing, construction, and commercial customers worldwide.

Industry: Industrial Machinery

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Davidson, United States

Founded: 1871

Website LinkedIn

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Ingersoll Rand

2 weeks ago

Quality Engineer

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 3 hours agoStatus: Live

Job Summary

Location: United States

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Own and maintain QMS processes including document control, change management, and quality record retention to ensure FDA/ISO and internal compliance.
•Develop and maintain procedures and work instructions in the electronic QMS (e.g., MasterControl).
•Support NPI and sustaining operations by ensuring validation deliverables (IQ/OQ/PQ), risk management, and regulatory/customer requirements are met.
•Investigate and resolve nonconformances using CAPA, including root cause analysis and effectiveness verification.
•Lead internal and external audits, ensuring audit readiness and timely closure of observations.

Pay and Benefits

Salary: USD 65,000 - 80,000 annually

Equity and Bonus:Equity

Perks:Health InsuranceDentalVision401kPaid LeaveLife InsuranceEquity

Key Requirements

•Bachelor’s degree (BA/BS) in Engineering, Quality, Life Sciences, or a related technical field.
•1–3 years of experience in Quality Engineering, Quality Systems, or a similar role in a medical device or regulated manufacturing environment.
•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 QMS (e.g., MasterControl) and strong technical writing/documentation skills (SOPs, work instructions, validation documents, quality records).

Experience:1-3 yearsMedical deviceRegulated manufacturingLife sciences

Education:Bachelor's

Skills:Technical writingDocumentationContinuous improvementRisk management

Certifications:Lead Auditor Certification

Tech Stack:MasterControlQMSElectronic QMSMicrosoft OfficeExcelWordPowerPoint

Company Brief

Ingersoll Rand

Industry: Industrial Machinery

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Davidson, United States

Founded: 1871

Website LinkedIn