Lab Technician
Axelon Services Corporation - Covington, GA
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Summary: Location: Covington, GA Duration: 6 Months Shift: 9:00am - 6:00pm, Monday through Friday Work Mode: In-Office Responsibilities: Represent the company, Division, and Quality Department professionally. Support Project Teams and Quality Department. Responsible for all product testing in the Complaint Laboratory. Provide Quality Engineering technical support to resolve quality issues, including complaint review. Perform complaint investigations for all UCC products and OEM manufactured products. Create investigation files in the complaint system (Trackwise). Set up, operate safely, and maintain laboratory equipment and testing instruments. Perform tests and experiments in accordance with GMP and GLP requirements. Develop and maintain knowledge of UCC policies, procedures, ISO, and FDA requirements. Maintain accurate data, analyze, and assist in drawing conclusions. Work in a biohazard environment and comply with safety policies and procedures. Ensure compliance with Department and Division procedures. Interface with manufacturing facilities, suppliers, and Product Legal Manufacturer (PLM) groups. May present data findings to peers, engineering, and management staff. Requirements: Basic knowledge of medical device regulation, industry or international standards. Good laboratory skills and working knowledge of laboratory bench methods and equipment. Understanding of laboratory instrumentation. Understanding of OSHA requirements, Quality Systems Regulations (QSR), GLP, ISO, AAMI, and FDA Guidelines. Excellent communication skills (verbal, written, and presentation). Ability to manage time and priorities effectively to meet deadlines. Ability to handle multiple task assignments. Ability to interpret Corporate, Division, and Department Procedures. Ability to work with minimal supervision. Preferred Skills: Technical or Associate degree in a science field is a plus. Prior laboratory experience desirable. American Society of Quality (ASQ) certification (CQE, CQA, CQM, etc.) is a plus. Proficiency with using MS Excel (pivot tables, v-lookup, etc.). Minimum 1 to 3 years of experience with regulated industry, including co-op/internship experience.
Created: 2026-04-15