QUALITY ASSURANCE ENGINEER
IN LAKELAND, FL, USA!
Date Posted: 08/15/2025
Hiring Organization: Rose International
Position Number: 487055
Industry: Medical Equipment & Supplies
Job Title: Quality Assurance Engineer
Job Location: Lakeland, FL, USA, 33815
Work Model: Onsite
Shift: Mon-Fri,4:45 AM - 7:30 PM
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 65
Min Hourly Rate($): 58.00
Max Hourly Rate($): 63.00
Must Have Skills/Attributes: Design, Quality Assurance, Testing
Experience Desired: developing and implementing process control, process improvement, testing, and inspection methods (5+ yrs)
Required Minimum Education: Bachelor's Degree
**C2C is not available**
Job Description
Required Education:
Bachelor's Degree or Higher
Required Qualifications/Skills/Experience:
5+ years of experience in developing and implementing process control, process improvement, testing, and inspection methods to ensure product quality
Ability to analyze defects, identify trends, recommend corrective actions, and collaborate with suppliers to resolve quality issues
Quality Assurance Engineer Responsibilities:
Develop and implement methods and procedures for process control, process improvement, testing, and inspection to ensure products meet quality standards and function as designed.
Design and install sophisticated testing equipment; perform product testing and analysis to maintain quality levels and minimize defects.
Analyze reports and defective products to identify trends, determine root causes, and recommend corrective actions.
Collaborate with suppliers to address quality issues, implement effective corrective measures, and support supplier quality improvement programs.
Work independently as an individual contributor, applying professional judgment and expertise with minimal supervision.
Utilize strong understanding of discipline-specific procedures and concepts, making informed decisions based on best practices and prior experience
Industry:
Medical Device Manufacturing
Estimated Start Date:
9/1/2025
Dress code:
Casual attire
**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 . Should you have any questions/concerns, via our secure .
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' .
IN LAKELAND, FL, USA!
Date Posted: 08/15/2025
Hiring Organization: Rose International
Position Number: 487055
Industry: Medical Equipment & Supplies
Job Title: Quality Assurance Engineer
Job Location: Lakeland, FL, USA, 33815
Work Model: Onsite
Shift: Mon-Fri,4:45 AM - 7:30 PM
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 65
Min Hourly Rate($): 58.00
Max Hourly Rate($): 63.00
Must Have Skills/Attributes: Design, Quality Assurance, Testing
Experience Desired: developing and implementing process control, process improvement, testing, and inspection methods (5+ yrs)
Required Minimum Education: Bachelor's Degree
**C2C is not available**
Job Description
Required Education:
Bachelor's Degree or Higher
Required Qualifications/Skills/Experience:
5+ years of experience in developing and implementing process control, process improvement, testing, and inspection methods to ensure product quality
Ability to analyze defects, identify trends, recommend corrective actions, and collaborate with suppliers to resolve quality issues
Quality Assurance Engineer Responsibilities:
Develop and implement methods and procedures for process control, process improvement, testing, and inspection to ensure products meet quality standards and function as designed.
Design and install sophisticated testing equipment; perform product testing and analysis to maintain quality levels and minimize defects.
Analyze reports and defective products to identify trends, determine root causes, and recommend corrective actions.
Collaborate with suppliers to address quality issues, implement effective corrective measures, and support supplier quality improvement programs.
Work independently as an individual contributor, applying professional judgment and expertise with minimal supervision.
Utilize strong understanding of discipline-specific procedures and concepts, making informed decisions based on best practices and prior experience
Industry:
Medical Device Manufacturing
Estimated Start Date:
9/1/2025
Dress code:
Casual attire
**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 . Should you have any questions/concerns, via our secure .
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' .
Job ID: 489696654
Originally Posted on: 8/16/2025
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