Lab Testing Specialist- 1st Shift

Noble Biomaterials•Scranton, PA

1d•Onsite

About The Position

Noble Biomaterials, Inc is currently seeking a Lab Testing Specialist for our 1st shift. The Lab Testing Specialist performs lab tests to ensure the quality of raw materials and finished products. The role also includes data entry, GMP documentation review, and verification of test results. This position helps maintain GMP compliance and ensures accurate, reliable laboratory records and reports. Employees in this position may be assigned to different work areas or job duties based on production demands. Applicants should be comfortable learning new tasks and adapting to changing priorities.

Requirements

High school diploma or GED required.
Experience in quality control or testing, ideally in a manufacturing environment.
Strong troubleshooting and problem-solving skills
Ability to work independently and stay organized
Proficient in Excel, Word, and Outlook.
Strong attention to detail and accuracy.
Clear written and verbal communication skills.
Work in varied indoor conditions which may include heat, cold, dust, loud noise, etc., with the use of personal protective equipment (PPE)
Age 18+

Nice To Haves

Familiarity with data entry, GMP documentation, and data verification is preferred.
Reliable transportation

Responsibilities

Perform routine and non-routine testing of raw materials, in-process materials, and finished products.
Conduct physical and electrical testing and maintain accurate test records.
Calibrate and maintain laboratory equipment.
Compile, analyze, and interpret test data to ensure products meet specifications.
Document all testing activities, including logbooks, data forms, and inventory records.
Identify quality issues, investigate questionable results, and recommend corrective actions.
Ensure all testing follows established methods, protocols, and GMP requirements.
Support failure investigations and process improvements.
Perform additional tasks as assigned by leadership.
Enter lab and production data accurately into electronic systems.
Review GMP documentation for completeness and compliance.
Verify data against source documents and report discrepancies.
Escalate data or documentation issues when needed.