Laboratory Technician

ALOIS Solutions; Covington (GA); On-site; USD 42,000 - 54,000; Full time

Job summary

ALOIS Solutions in Covington, GA seeks Lab Technicians to support lab testing, investigations, and QA activities in a regulated medical device setting.

The ideal candidate has lab experience, GMP/GLP knowledge, and strong documentation skills to ensure compliant testing under FDA, ISO, and QSR standards.

Qualifications

• 1–3 years of experience in a regulated industry (internship or co-op acceptable).
• Prior laboratory experience and knowledge of bench methods.
• Understanding of laboratory instrumentation and testing equipment.
• Knowledge of GMP, GLP, FDA guidelines, ISO standards, and quality systems.
• Proficiency in Microsoft Excel, including Pivot Tables and VLOOKUP.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities, work independently, and maintain attention to detail.

Responsibilities

• Perform product testing in the Complaint Laboratory.
• Provide technical support to Quality Engineering teams in resolving quality issues and complaint investigations.
• Create and maintain investigation files using TrackWise.
• Safely operate, maintain, and utilize laboratory equipment and testing instruments.
• Perform laboratory testing in compliance with GMP and GLP.
• Maintain accurate test data, analyze results, and assist in drawing conclusions.
• Support compliance with FDA guidelines, ISO standards, OSHA requirements, and QSR.
• Collaborate with manufacturing facilities, suppliers, and PLM groups.
• Maintain accurate documentation and ensure compliance with procedures.

Skills

Lab testing

Regulatory knowledge

Quality systems

Written and verbal communication

Education

Tech/Assoc degree

ASQ CQE

ASQ CQA

Tools

Excel Pivot Tables

VLOOKUP

Job description

Client Industry: Medical Devices

Location: Covington, GA (Onsite)

Work Schedule: Monday – Friday | 9:00 AM – 6:00 PM

Open Positions: 2

Position Overview

We are seeking qualified Lab Technicians to support laboratory testing, complaint investigations, and quality assurance activities within a regulated medical device environment.

The ideal candidate will have laboratory experience, knowledge of quality systems, and the ability to perform testing and documentation in accordance with applicable industry standards and regulatory requirements.

Key Responsibilities

• Perform product testing in the Complaint Laboratory.
• Provide technical support to Quality Engineering teams in resolving quality issues and complaint investigations.
• Create and maintain investigation files using TrackWise.
• Safely operate, maintain, and utilize laboratory equipment and testing instruments.
• Perform laboratory testing in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Maintain accurate test data, analyze results, and assist in drawing conclusions.
• Support compliance with FDA guidelines, ISO standards, OSHA requirements, and Quality Systems Regulations (QSR).
• Collaborate with manufacturing facilities, suppliers, and Product Legal Manufacturer (PLM) groups.
• Maintain accurate documentation and ensure compliance with departmental procedures.

Required Qualifications

• 1–3 years of experience in a regulated industry, including relevant internship or co-op experience.
• Prior laboratory experience and knowledge of laboratory bench methods.
• Understanding of laboratory instrumentation and associated testing equipment.
• Knowledge of GMP, GLP, FDA guidelines, ISO standards, and quality systems.
• Proficiency in Microsoft Excel, including Pivot Tables and VLOOKUP.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities, work independently, and maintain attention to detail.

Preferred Qualifications

• Technical or Associate degree in a science-related field.
• ASQ certification, such as CQE, CQA, or CQM.