- Location: ME, United States
- Type: Contract
- Job ID: 10461
- Work Setting: On-Site
- Posted: July 13, 2026
- Closing Date: December 31, 2026
- Tax Status: W2
Quality Control Technician
5-month Contract
Onsite – Scarborough, ME
Must be able to work on a W2
Summary
Our client, a Fortune 500 Medical Device Company, has engaged GForce Life Sciences to provide a Quality Control Technician to support laboratory testing and quality operations for its Infectious Disease business unit. This role performs in-process and final release testing, maintains GMP/GLP compliance, and ensures products meet quality and regulatory standards.
Requirements
5-month Contract
Onsite – Scarborough, ME
Must be able to work on a W2
Summary
Our client, a Fortune 500 Medical Device Company, has engaged GForce Life Sciences to provide a Quality Control Technician to support laboratory testing and quality operations for its Infectious Disease business unit. This role performs in-process and final release testing, maintains GMP/GLP compliance, and ensures products meet quality and regulatory standards.
Requirements
- Perform in-process quality control testing for Lateral Flow, ELISA, and Molecular diagnostic products.
- Conduct final release testing to ensure products meet quality and regulatory requirements.
- Troubleshoot technical and quality-related issues and assist with root cause investigations.
- Perform laboratory procedures while following established SOPs and safety guidelines.
- Operate laboratory equipment and perform routine technical procedures.
- Review batch records for accuracy and completeness.
- Calibrate, maintain, and verify laboratory equipment.
- Maintain compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Accurately document laboratory activities, testing results, and quality records.
- Support Quality Management System (QMS) activities and continuous improvement initiatives.
- Recognize and report deviations from approved manufacturing or laboratory procedures.
- Maintain a clean, organized laboratory environment, including routine cleaning and sanitization activities.
- Collaborate with Quality, Manufacturing, and other cross-functional teams to support production and product quality.
- Associate’s or Bachelor’s degree in Biology, Chemistry, Life Sciences, or another related scientific discipline (or equivalent combination of education and experience).
- Minimum of 1 year of laboratory and/or Quality Control experience.
- Experience performing laboratory testing in a regulated environment.
- Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Ability to follow detailed procedures and accurately document results.
- Strong troubleshooting and problem-solving skills.
- Excellent attention to detail and organizational skills.
- Strong written and verbal communication skills.
- Proficiency with Microsoft Office applications, including Outlook, Word, and Excel.
- Familiarity with inventory, database, or manufacturing software.
- 2+ years of experience in a regulated medical device, pharmaceutical, biotechnology, or diagnostics environment.
- Experience working with FDA, ISO, and USDA regulations.
- Hands-on experience with, ELISA assays, Molecular diagnostic testing, Pipettes, pH meters, Immunochromatographic assays
- Experience with laboratory equipment calibration and maintenance.
- Knowledge of statistical analysis, data interpretation, and systematic troubleshooting techniques.
- Experience supporting Quality Management Systems (QMS) and product release activities.