Last updated 2026-07-05
169 Remote QA Engineering Jobs in the United States
Browse 169 remote QA Engineering jobs across the United States. Listings are updated hourly and include salary data where available.
Market data for QA Engineering jobs in the United States
Professionals focused on ensuring product quality, compliance, and process improvement across various engineering and manufacturing sectors.
Remote U.S. QA Engineering salary data
Salary figures are based on postings with disclosed compensation and are shown as annualized ranges when available.
Hourly remote QA Engineering roles in the United States pay a median rate of $58/hr based on 6 postings.
| Pay type | Low | Median | High |
|---|---|---|---|
| Annual | $113K | $140K–$172K | $217K |
| Hourly | $41/hr | $58/hr | $96/hr |
| Scope | P50 salary | P25-P75 range | Samples |
|---|---|---|---|
| Remote U.S. | $144K | $100K-$183K | 372 postings |
| U.S. | $118K | $85K-$159K | 6,486 postings |
Pay visibility: 95 of 169 visible postings include structured pay data (56%).
Companies with current QA Engineering listings
| Company | Active jobs |
|---|---|
| Otsuka Pharmaceutical Development and Commercialization, Inc. | 13 |
| Olympus Corporation of the Americas | 8 |
| Veeva | 7 |
| BeOne Medicines USA, Inc. | 6 |
| Parexel | 6 |
| Thermo Fisher Scientific | 6 |
| RTX | 5 |
QA Engineering jobs by schedule
QA Engineering jobs by seniority
Common QA Engineering job titles
FAQ
- How many QA Engineering jobs are listed in the United States?
- This page currently shows 169 QA Engineering jobs in the United States.
- What salary data is available for QA Engineering jobs in the United States?
- Salary comparison includes Remote U.S. ($144K P50, $100K-$183K P25-P75, 372 postings) and U.S. ($118K P50, $85K-$159K P25-P75, 6,486 postings).
- Which companies are hiring for QA Engineering roles in the United States?
- Current listings include roles from Otsuka Pharmaceutical Development and Commercialization, Inc. (13 jobs, 7%), Olympus Corporation of the Americas (8 jobs, 4%), Veeva (7 jobs, 4%), BeOne Medicines USA, Inc. (6 jobs, 3%), and Parexel (6 jobs, 3%).
- What seniority levels are common for QA Engineering jobs in the United States?
- The visible seniority mix includes Senior (102 jobs, 60%), Mid (66 jobs, 39%), and Entry (1 job, 1%).
- What work schedules are common for QA Engineering jobs in the United States?
- The visible schedule mix includes Full time (165 jobs, 98%), Contract (3 jobs, 2%), and Part time (1 job, 1%).
- What QA Engineering job titles are common in the United States?
- Common titles include Regulatory Affairs Manager (3 jobs, 2%), Associate Director, Drug Product & Process Development (Small Molecules) (2 jobs, 1%), Associate Director, Drug Product Development (2 jobs, 1%), Associate Director, Regulatory Affairs, CMC (2 jobs, 1%), and CMC Consultant (2 jobs, 1%).
- What does this market snapshot include?
- Most visible listings are full-time (165 of 169). Senior-level roles account for 102 of 169 listings. 95 of 169 visible postings include structured pay data.
Related remote jobs
Snapshot updated 1hr, 25m ago
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- Essential Functions of the job: With minimal supervision, plan and manage regulatory activities related to assigned projects that span tech…
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- Manager, Biologics Analytical Development (Bioassay) will execute and support the development, qualification, and lifecycle management of b…
- Qualifications & Experience Education PhD in Biology, Biochemistry, Immunology, Bioengineering, or a related discipline Experience 8–10+ ye…
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RTX
Jul 2- Proficiency with audit management software and tools.
- Minimum of 5 years of experience in quality assurance, with at least 3 years in QMS auditing within the aerospace,…
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Zimmer, Inc.
Jul 2- Serve as the primary Regulatory Affairs liaison for IT-related initiatives, partnering closely with cross-functional teams to represent reg…
- Lead the intersection of Regulatory Affairs and IT by serving as the key regulatory representative for technology-driven initiatives.
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NRG
Jul 2- This role, situated on the Sales Quality team center of excellence, leverages a proprietary set of tools, processes, and data…
- Perform daily reviews of assigned Quality reports and follow up as necessary.
- Demonstrates knowledge and experience working with: Various regulations (HIPPA, EU-MDR, FDA 21 CFR Part 803, 806, 820) Various standards (G…
- Cross-functional meetings: Uses Medical subject matter expertise to represent Medical Safety in cross-functional meetings related to HHA, F…
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Dentsply Sirona, Inc
Jul 2- Knowledge of regulatory affairs principles and practices.
- Key Responsibilities : Develops and implements regulatory strategies to obtain and maintain regulatory approvals for medical devices and ot…
Thermo Fisher Scientific
Jul 2- In this role, you will lead project management activities across a portfolio of client programs, partnering closely with technical, analyti…
- This individual will help establish and continuously improve project management processes, support team prioritization, proactively identif…
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Veeva Systems
Jul 2- What You'll Do Act as subject matter expert for the Document Control process area by owning the lifecycle management of…
- Serving as the process owner for document control, this role ensures processes are defined, monitored, assessed, and maintained across mult…
Symbotic
Jul 1- Manager, Manufacturing Quality Implementation & Quality Management | USA Remote & Travel Apply Project Manager, Layout Engineering (Central…
- By partnering cross-functionally across Engineering, Manufacturing, Supply Chain, and Test teams, they embed strong quality practices, qual…
Spyre Therapeutics
Jul 1- The Senior Manager, GCP Quality will support Clinical Quality Assurance (CQA) activities across Spyre’s clinical development programs, incl…
- This role requires strong knowledge of GCP regulations and quality systems, as well as the ability to collaborate effectively across…
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Flourish Research
Jul 1- We are actively hiring a remote QC & Data Management Specialist I LOCATION : Remote FLSA : Non-Exempt HOURS :…
- Assists with key initiatives/process improvements in the department.
- Job Description Roles and Responsibilities Business Process Management Systems (e.g. Quality Management Systems, Integrated Management Syst…
- Required Qualifications For roles outside of the USA- This role requires significant experience in the Quality & Business Process Managemen…
- Regularly advises management in Central Quality.
- This includes scheduling, preparation, execution, reporting, and follow-up activities associated with Central Quality & Regulatory Internal…
- The Regulatory and Clinical Specialist is a liaison with the organization working with various groups to effectively communicate and collab…
- Responsible for regulatory authority queries on clinical evaluation Support the Compliance Review Board process by reviewing promotional ma…
1001 Syneos Health, LLC
Jul 1- Job Responsibilities Core Responsibilities: Line management of Clinical Operations staff, responsibilities including interviewing and selec…
- Bachelor’s degree in life sciences, nursing degree, or equivalent related experience, plus extensive clinical research experience in a cont…
GE HEALTHCARE
Jul 1- Regularly advises management in Central Quality.
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CannonDesign
Jun 30- Regulatory Expertise and Compliance Ensure adherence to local, state, and federal regulations, including safety codes and healthcare-specif…
- Identify potential regulatory compliance risks/issues and provide recommendations for mitigation strategies.
Secura Bio
Jun 30- About the Role The Manager of Document Control and Training is responsible for overseeing the document control and training processes…
- Responsible for supporting and overseeing Document Control activities for documents used in GxP operations (includes manufacturing, clinica…
Bbraun
Jun 30- The Specialist acts as a healthcare sterile processing and surgical instrumentation experts who bring innovative solutions and improvements…
- 4 - 6 years’ experience in Peri-operative Services or Healthcare Sterile Processing preferred or related industry experience.
AppliedVR
Jun 30- Reporting to the Director of QA/RA and working closely with Product and Engineering stakeholders, the initial focus of the Quality…
- Cross-Functional Leadership: Act as the Quality partner across Product, Engineering, and SQE teams to drive consistent understanding, adopt…