Quality Assurance Engineer

Overview

On Site
Hybrid
USD 28.96 per hour
Full Time

Skills

Recruiting
Health Care
Risk Management
Six Sigma
Lean Methodology
Statistics
ISO 13485
ISO 9000
Microsoft Office
Microsoft Excel
Microsoft PowerPoint
Microsoft Outlook
Microsoft Windows
Network
File Systems
Adaptability
Work Ethic
Data Analysis
Attention To Detail
Organized
Multitasking
Project Management
Distribution
Technical Support
Continuous Improvement
Root Cause Analysis
Corrective And Preventive Action
Quality Management
Reporting
Manufacturing
Auditing
Quality Assurance
Sales

Job Details

Date Posted: 08/13/2025

Hiring Organization: Rose International

Position Number: 486918

Industry: Healthcare

Job Title: Quality Assurance Engineer

Job Location: Skaneateles Falls, NY, USA, 13153

Work Model: Hybrid

Work Model Details: 50% Onsite, 50% Remote

Shift: First Shift

Employment Type: Temporary

FT/PT: Full-Time

Estimated Duration (In months): 4

Min Hourly Rate($): 28.96

Max Hourly Rate($): 31.11

Must Have Skills/Attributes: Data Analysis, FDA, ISO 13485, Six Sigma

Experience Desired: Experience within a manufacturing environment and data analytics (3+ yrs); Experience reading and understanding blueprints and other technical data (3+ yrs); Experience working with FDA regulations (3+ yrs); Experience with manufacturing/quality methodologies (3+ yrs); Experience with formal quality systems such as ISO 13485 or ISO 9001 (3+ yrs)

Required Minimum Education: Bachelor's Degree

Preferred Certifications/Licenses: ASQ or related quality certifications

**C2C is not available**

Job Description
50% Onsite, 50% Remote

Education:
Bachelor's in Engineering
ASQ or related quality certification is preferred.

Requirements:
3+ years relevant work experience
Prior experience within a manufacturing environment and data analytics
Demonstrated ability to analyze, evaluate, and control risk following lifecycle risk management standards (e.g. ISO 14971)
Experience with manufacturing / quality methodologies such as QFD, six-sigma, lean, etc.
Understanding of statistical analysis techniques and tools.
Experience with formal quality systems such as ISO 13485 or ISO 9001.
Proficient in the use of Microsoft Office tools such as Word, Excel, PowerPoint, Outlook, etc.
Comfortable with using PC tools and Windows OS, with a working knowledge of local and network based file systems.
Able to be flexible and adaptable when needs and priorities change Physical demands and work environment

Top Skills:
Ability to work unsupervised, strong work ethic, self-starter
Experience working with data, comfortable with data analysis
Comfortable reading and understanding blueprints and other technical data
Strong interpersonal skills and attention to detail
Organized and able to multitask.

Nice to Have Skills:
Project management experience
Experience working with FDA regulations or other regulated fields
Supplier quality experience

Job Duties:
Quality Assurance Engineer will be working closely with the supplier quality team to address gaps within supplier quality and distribution systems.
They will be expected to pull and review data and work with internal and external groups to implement solutions.
The Quality Assurance Engineer provides technical support for various quality system processes to help ensure excellent product quality throughout product lifecycles.
Drive continuous improvement actions focused on product quality.
Works with Engineering and Manufacturing to develop acceptance criteria for production processes.
Works with Service and the Complaint Handling Unit to investigate product problems, perform root cause analysis and identify possible corrective actions.
Analyzes production quality data to identify trends or issues which require action or CAPA activity.
Assists in creating and implementing procedures in the quality management system.
Assists in the review and disposition of nonconforming materials.
Assists in the creation and validation of manufacturing processes.
Conducts internal audits of production processes and report results.
Reviews manufacturing process and part deviations.
Creates quality alerts when acceptance activities need to be adjusted.
Supports external regulator or customer audits
Provides response to inquiries related to quality assurance arising from tenders or other sales efforts.

  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.**


Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.


California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.


Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
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