Laboratory Technician job in Covington
Covington CorTech LLC
| Job Ref: | 372172 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 26.00-26.00/Per Hour |
| Remote: | No |
Location |
|
| City: | Covington |
| Post Code: | 30014 |
| Map: |
|
Description |
|
|
Schedule: M-F 9Am-6Pm Pay: $26.00 hourly Location: on-site Weekly pay Health benefits 401k Are you passionate about quality, precision, and making a real impact in a regulated industry? Join our team and play a vital role in ensuring product safety and reliability in a hands-on laboratory environment. As a Quality Laboratory Specialist, you will be a key representative of the Quality Department, supporting cross-functional teams while driving product testing and complaint investigations. Your work will directly contribute to maintaining the highest standards of compliance, quality, and patient safety. What You?ll Do Perform product testing and analysis within the Complaint Laboratory to support investigations and quality initiatives Lead and support complaint investigations for UCC and OEM products, ensuring accurate documentation in Trackwise Provide technical Quality Engineering support to resolve product and process issues Set up, operate, and maintain laboratory equipment and testing instruments safely and effectively Conduct testing in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) Analyze data, interpret results, and communicate findings to cross-functional teams and leadership Collaborate with manufacturing sites, suppliers, and Product Legal Manufacturer (PLM) groups Ensure compliance with internal procedures, ISO standards, OSHA requirements, and FDA regulations Maintain detailed and accurate records with a strong focus on data integrity and attention to detail Present findings and recommendations to peers, engineering teams, and management as needed What You Bring Associate or technical degree in a science-related field preferred 1?3 years of experience in a regulated industry (internships/co-ops included) Hands-on laboratory experience and familiarity with laboratory instrumentation Working knowledge of medical device regulations, ISO standards, and FDA guidelines Proficiency in Microsoft Excel (including pivot tables and VLOOKUP) Strong analytical, organizational, and problem-solving skills Ability to manage multiple priorities and meet deadlines with minimal supervision Excellent communication skills, both written and verbal ASQ certification (CQE, CQA, CQM, etc.) is a plus Why You?ll Love This Role Work in a dynamic, regulated environment where your contributions truly matter Gain exposure to quality systems, regulatory standards, and cross-functional collaboration Play a direct role in supporting product quality and patient safety Grow your technical expertise and advance your career in quality and laboratory operations BD04123JD | |
ref: (372172)
less than 2 minutes ago
Back to search results