Quality Assurance (QA) Specialist I

The Fountain Group is currently seeking a Quality Assurance Specialist I for a prominent client of ours. This position is located in North Chicago, IL. Details for the position are as follows: Pay: $25-28/hr. 6-month assignment with possibility for extension or conversion based on performance and budget. Responsibilities: Perform product complaint documentation, investigation, and review of all non-medical complaint content. Analyze and test routine to medium complexity products, and evaluate results. Performs test methods as written to support product complaint investigation activities. Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GLP. This requires good analytical skills, technical writing, and good documentation. Responsible for complaint data meeting all regulatory requirements. Identification and initiation of appropriate exception documents in accordance with procedural requirements; supports the investigation processSupports redline changes to local documents; Supports team to meet broader business objectives; Assists in projects and activitiesBudgets their time with minimal supervision to effectively carry out assigned tasks and proposes improvements to processes across the QA lab. Takes initiative to be a key player in team activities. Understands, implements, and maintains a safe work environment and good manufacturing practices with respect to procedural requirements and laboratory records and requirements. Maintains lab for safety and compliance. Maintains training certificates as needed for assigned job tasks. Interprets data results for conformance with expected results as defined per proceduresUnderstands laboratory techniques and principles performed and can independently troubleshoot and resolve analytical techniques and instrument issues. Understands, implements and maintains GxP with respect to laboratory records, procedures and systems in accordance with procedural requirements Qualifications: Bachelor's degree in science or technologyBackground in medical device is preferredQuality control background within a cGMP environment is highly preferredExperience with sample testing/sample management preferred If you are interested in hearing more about the position, please respond to this posting with your resume attached. Please forward this posting to any friends or colleagues as we do offer a Referral Bonus for any candidate hired. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy