NEW JOB OPENING
QUALITY ENGINEER
IN Mahwah, NJ, USA!

 

Date Posted: 07/23/2026
Hiring Organization: Rose International
Position Number: 504591
Industry: Medical Equipment & Supplies
Job Title: Quality Engineer
Job Location: Mahwah, NJ, USA, 07430
Work Model: Hybrid
Work Model Details: Hybrid Minimum 3 days onsite
Shift: 8am-5pm M-F - Hybrid - Minimum 3 days onsite
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 13
Min Hourly Rate($): 50.00
Max Hourly Rate($): 50.00
Must Have Skills/Attributes: Analytical Skills, Change Management, SOP
Experience Desired: Experience supporting quality activities within a manufacturing environment (1 yrs); Knowledge of Quality Management Systems (QMS) and change management processes (1 yrs); Experience supporting Product Transfers and Supplier Change Requests (1 yrs)
Required Minimum Education: Bachelor’s Degree

**C2C is not available**

 

Job Description
Required Education:

• Bachelor’s Degree in Biomedical Engineering, Mechanical Engineering, or related field.



Required Qualifications:

• Minimum 1 year of Quality Engineering or Manufacturing Engineering experience.

• Knowledge of Change Management and Quality Management Systems (QMS).

• Strong analytical, troubleshooting, and problem-solving skills.

• Excellent written and verbal communication skills.

• Strong organizational skills with exceptional attention to detail.

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

• Ability to manage multiple priorities in a fast-paced manufacturing environment.

• Ability to work independently while collaborating effectively with cross-functional teams.

• Up to 10% travel as required.



Preferred Qualifications:

• Experience in the medical device industry.

• Working knowledge of:

• ISO 13485

• GMP (Good Manufacturing Practices)

• GDP (Good Documentation Practices)

• Experience supporting:

• Product Transfers

• Supplier Change Requests

• PPAP

• Process Validation (IQ/OQ/PQ)

• First Article Inspection (FAI)

• Risk Management

• Statistical analysis and process capability

• Familiarity with CAPA, nonconformance investigations, and continuous improvement methodologies.



Job Summary:

• Support quality assurance, quality control, and continuous improvement activities within a medical device manufacturing environment.

• Ensure products meet quality, regulatory, and customer requirements throughout the manufacturing process.

• Lead and support Product Transfers, Supplier Change Requests, PPAP, First Article Inspection (FAI), and validation projects.

• Develop, implement, and maintain quality processes, inspection methods, and manufacturing controls.

• Create and update Standard Operating Procedures (SOPs) and inspection plans through the change management system.

• Collaborate with Engineering, Manufacturing, Supply Chain, and Operations to resolve quality issues and improve processes.

• Serve as the quality representative on cross-functional projects, ensuring compliance with Quality Management System (QMS) requirements.

• Support compliance with ISO 13485, GMP, GDP, and other applicable regulatory standards.

• Investigate quality issues, perform root cause analysis, and drive corrective and preventive actions (CAPA).

• Promote continuous improvement initiatives that enhance product quality, manufacturing efficiency, and customer satisfaction.

• Work independently while exercising sound engineering judgment and professional decision-making.

• Build strong cross-functional relationships and serve as the voice of Quality across the organization.





  • **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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About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.

Diane, Consultant

Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.

David, Consultant

I had a very positive experience working for Rose. The entire process is very efficient and easy.

Joanne, Consultant

Rose is an assembly of people grounded in honesty, truth and dignity for all of its employees and contractors.

Samba, Consultant

Rose International has been great to me. I thank everyone there for all of their hard work; it has not gone unnoticed.

Melody, Consultant

EMPLOYEE COMMENTS

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