Senior Specialist Quality Assurance
AbbottAbout the role
JOB DESCRIPTION:
Senior Specialist Quality Assurance
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:
Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
At Molecular Diagnostics, we realize the potential of personalized care as the laboratory’s most trusted and preferred source for molecular diagnostic solutions. We are a division of Abbott Laboratories, a global, diversified healthcare innovator with a legacy of pioneering work in medical diagnostics.
The Senior Specialist, Quality Assurance role is part of our Molecular Diagnostics Business Unit and is based at either our Des Plaines, IL or Lake Forest, IL location.
This role will conduct quality-related activities in the area of Complaint Handling to deliver consistent, high-quality documents, services, products, and processes that add value to the business. The primary function of the Quality Specialist is to assist in maintaining the quality system.
What You’ll Work On
- Complaints Coordination, Postproduction Risk, CAPA, Surveillance and Maintenance, Field Actions, Metrics, etc.
- Assist with other support duties as assigned.
- Participate in the Corrective Action/Preventive Action (CAPA) process, including the investigation of failures or deviations as required.
- Maintain product complaint logs to identify and report recurring issues to Quality Assurance Management and Product Development. Collaborate with other internal groups to respond to product inquiries and issues.
- Write and revise SOPs, controlled forms, and related documents to ensure best practices and alignment with current operations.
- Collaborate with members of the Quality Assurance team working on special projects.
- Participate on permanent and temporary teams that are process- or project-driven.
- Become familiar with and serve as a subject matter expert on electronic support systems, including TraqWise, CMSNext, SmartSolve, SAP, and related platforms.
- Collect, analyze, and publish quality metrics.
- Assist in the preparation of distribution reports as needed for product information letters and field actions.
- Support the drafting of field action letters and other field action-related documentation.
- Reconcile and maintain field action files, ensuring all documentation is complete and appropriately filed in accordance with corporate/division standards to facilitate easy retrieval for audit support.
- Prepare 806 monthly status reports in support of 21 CFR Part 806 field action requirements.
- Track recall activities through closure and prepare final closure documentation for each field action file.
- Support audit readiness activities for internal (site, division, and corporate) and external (FDA, ISO, BSI, TUV, etc.) audits.
- Handle data requests from other departments pertaining to risk or field action data.
- Serve as a team member and/or leader on projects focused on continuous
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