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Quality Assurance Coordinator

Insight Global

Mundelein, ILJobNo compensation foundTracked 2w agoSeen in employer's feed 4 days ago

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At a glance

Compensation
No compensation found
Location
Mundelein, IL
Work Authorization
Not specified

Job overview

Insight Global is hiring a Quality Assurance Coordinator. Insight Global seeks detail‑oriented professionals to support a medical device client in Mundelein, IL, handling customer complaints, product inquiries, and recall activities while providing phone and email support, coordinating returns, maintaining documentation, and ensuring FDA regulatory compliance.

Important skills include Microsoft Office, Outlook, Microsoft Word, Excel, Zendesk, and Genesys.

Skills & qualifications

RequiredNice to have

Skills

Microsoft OfficeOutlookMicrosoft WordExcelZendeskGenesysCommunicationPhone SupportEmail SupportAttention to DetailDocumentation SkillsReport GenerationReport AnalysisOrganizedAdaptableCustomer-Focused Phone PresenceFDA Regulations Knowledge21 CFR 806 KnowledgeISO 13485 Knowledge

Qualifications

Associate's Degree2+ Years Customer Service ExperienceComplaint Handling ExperienceQuality Assurance ExperienceProduct Recalls ExperienceDocumentation Management ExperienceRegulated Industry ExperienceMedical Device Industry ExperiencePharmaceutical Industry Experience

Full job description

Job Description

Insight Global is seeking detail-oriented professionals to support an established medical device client in the Mundelein, IL area. This team serves as the primary point of contact for customer complaints, product inquiries, and recall-related activities. Individuals will provide phone and email support, coordinate product return processes, maintain detailed documentation, and ensure regulatory compliance with FDA requirements.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Skills and Requirements

  • Associate's degree preferred

  • 2+ years of relevant experience in customer service, complaint handling, quality assurance, product recalls, or documentation management

  • Experience in a regulated industry, preferably medical device or pharmaceutical

  • Strong verbal and written communication skills with experience providing phone and email support

  • Experience handling customer complaints, product inquiries, or recall-related issues

  • Strong attention to detail and documentation skills in a regulated environment

  • Proficiency with Microsoft Office, including Outlook, Word, and Excel

  • Ability to learn and navigate internal tracking and reporting systems

  • Organized, adaptable, and able to manage multiple customer interactions and priorities

  • Professional, customer-focused phone presence with the ability to communicate clearly and provide detailed instructions

Experience maintaining accurate records and documentation in accordance with FDA requirements • Experience with Zendesk, Genesys, or similar customer support platforms

  • Medical device, pharmaceutical, distribution, or retail customer support experience

  • Experience generating and analyzing reports

Familiarity with FDA regulations, including FDA 21 CFR 806 and ISO 13485

You've read the whole posting — now see how you match it.