Senior In Vitro Lab Technician - GLP/ISO Specialist

North American Science Associates, Inc.; Northwood (OH); On-site; USD 55,000 - 85,000; Full time

Job summary

You will communicate with clients and study directors, organize schedules, manage reagents, and ensure proper documentation and chain-of-custody. This role demands meticulous data handling in a GMP/GLP environment and regular equipment maintenance.

Qualifications

• Bachelor’s degree in scientific discipline with at least two years of lab experience.
• Three years’ experience in a laboratory setting, preferably in a GLP environment.
• Experience following GMP/GLP guidelines and applicable regulations.

Responsibilities

• Strictly adheres to GLP guidelines and conducts audits.
• Performs routine testing per NAMSA SOPs with data analysis.
• Maintains cell lines, propagation, viability, and plate preparation.
• Executes ISO 10993, USP, and JMHLW compliant extraction processes.
• Communicates with clients regarding observations or article abnormalities.
• Routinely communicates with Study Directors and QA about issues, results, or audits.
• Creates, communicates and implements schedules for Associates for lab workload.
• Performs data entry, calculations, analysis and routes results for review.
• Prepares and maintains reagents/test articles and sterile glassware.
• Maintains ancillary records and equipment, and monitors lab environment.

Skills

GLP compliance

Cytotoxicity

Hemocompatibility

Genotoxicity

Technical writing

Education

Bachelor’s degree in scientific discipline

High school diploma with 6+ years lab experience

Tools

LIMS

TrackWise

MasterControl

Job description

You will communicate with clients and study directors, organize schedules, manage reagents, and ensure proper documentation and chain-of-custody. This role demands meticulous data handling in a GMP/GLP environment and regular equipment maintenance.