Job Title: Quality Associate II Location: Deerfield, IL Hybrid

Duration: Months

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 ( Minitab, Excel). Degree in Engineering or Life Sciences

Requires minimum years of experience in Quality, Manufacturing, Engineering in Medical Device industry.