Overview
On Site
Accepts corp to corp applications
Contract - W2
Contract - to 07/26/2026
Skills
Profit And Loss
Surveillance
Documentation
Quality Management
Management
Manufacturing
Supervision
Analytical Skill
Conflict Resolution
Problem Solving
Microsoft Office
Data Collection
Minitab
Microsoft Excel
Life Sciences
Manufacturing Engineering
Medical Devices
Job Details
Description:
Hybrid in DF
Essential Duties and Responsibilities:
Provide post market surveillance support by owning and resolving issues within complaint trending
Define product families and their associated problem codes and components to improve complaint handling and complaint trending
Update documentation and quality systems impacting complaints and complaint trending
Manage activities of self and support others in achieving defined quality goals in an efficient, accurate and timely manner.
Qualifications:
Ability to engage management and other functions to influence decisions on courses of action with minimal assistance using both written and verbal methods.
Demonstrate understanding and working knowledge in the areas of worldwide Quality System standards and regulations, including FDA Regulations and Application of Good Manufacturing Practices.
Ability to work under deadlines and changing priorities with minimal supervision.
Strong analytical and problem-solving skills.
Must be proficient with Microsoft Office and other data collection/analysis programs (e.g. Minitab, Excel).
B.S Degree in Engineering or Life Sciences
Requires minimum 2 years of experience in Quality, Manufacturing, Engineering in Medical Device industry.
Are Workers Project-based? Essential Duties and Responsibilities:
Provide post market surveillance support by owning and resolving issues within complaint trending
Define product families and their associated problem codes and components to improve complaint handling and complaint trending
Update documentation and quality systems impacting complaints and complaint trending
Manage activities of self and support others in achieving defined quality goals in an efficient, accurate and timely manner.
Qualifications:
Ability to engage management and other functions to influence decisions on courses of action with minimal assistance using both written and verbal methods.
Demonstrate understanding and working knowledge in the areas of worldwide Quality System standards and regulations, including FDA Regulations and Application of Good Manufacturing Practices.
Ability to work under deadlines and changing priorities with minimal supervision.
Strong analytical and problem-solving skills.
Must be proficient with Microsoft Office and other data collection/analysis programs (e.g. Minitab, Excel).
B.S Degree in Engineering or Life Sciences
Requires minimum 2 years of experience in Quality, Manufacturing, Engineering in Medical Device industry.
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