Overview
Quality Assurance Specialist Jobs in North Chicago, IL at Intellectt Inc
Title: Quality Assurance Specialist
Company: Intellectt Inc
Location: North Chicago, IL
Role: QA Specialist I
Location: Abbott Park, IL- 60064-3500
Duration: 5 Months
Shift Timings: 8 to 4:30
100% onsite role
Job Description:
The Specialist Quality Assurance within the Diagnostics Division will analyze quality standards for components, materials or services.
Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met.
Design/Change Control – Responsibilities include participating in the development & review of all design input, risk management, design verification, design validation and design output/transfer related design change activity.
Risk Management – Understands and applies basic Risk Management principles.
Participates in the development and/or modification of Risk Management Files, FMEA, etc.
Design Verification/Validation – Understands and applies basic Design Verification/Validation methods & principles.
Participates in the development, modification and design review of
Protocols, Data Summaries & Records.
Documentation – Reviews documentation for accuracy, clarity, consistency, completeness and compliance for projects that vary from low to high complexity.
Plans and performs assignments with a wide degree of difficulty.
Quality System Compliance -Maintains awareness of standards that regulate our industry.
Ensures compliance to site level policies and procedures by promptly reporting non-compliance issues to management within Division and Corporation as appropriate.
Maintains vigilance to ensure adherence to Quality Policy and Quality system procedures by promptly reporting noncompliance issues to management.
Quality Engineering – Participates on project teams and technical review boards.
Coordinates quality decisions between different quality and engineering groups.
Effectively navigates & facilitates project teams with respect to our processes and procedures ensuring the delivery of safe and effective products.
Apply quality principles, analyze quality records, prepare reports and recommend improvements.
Conduct inspection, verification and validation of components or materials used in development processes.
Document quality issues and performance measures for management review.
Required
Bachelor’s Degree Required
Preferred
Knowledgeable of FDA, Quality System Regulations (QSR), Medical Device Directive, ISO guidelines and 21 CFR Part 11
Interview
2 rounds of interview (first round will be video and second round will be onsite)
