GLP

Term from Laboratory Testing industry explained for recruiters

GLP (Good Laboratory Practice) is a quality system for laboratories that ensures consistency, reliability, and accuracy in non-clinical laboratory studies and tests. Think of it as a set of rules and standards that laboratories must follow to make sure their work is trustworthy and properly documented. It's especially important in industries like pharmaceutical testing, chemical safety studies, and environmental monitoring. When you see GLP mentioned in a resume, it means the person understands and has worked within these important laboratory quality guidelines.

Examples in Resumes

Managed GLP compliant laboratory testing procedures for pharmaceutical products

Conducted environmental safety studies following GLP standards

Supervised a team of 5 technicians in GLP and Good Laboratory Practice certified facility

Typical job title: "Laboratory Technicians"

Also try searching for:

Lab Technician Quality Control Specialist Laboratory Manager Research Associate Quality Assurance Specialist Laboratory Analyst GLP Study Director

Example Interview Questions

Senior Level Questions

Q: How would you handle a situation where you discover a GLP non-compliance issue in your lab?

Expected Answer: A senior professional should discuss the importance of immediate documentation, proper reporting procedures, implementing corrective actions, and preventing future occurrences. They should also mention the importance of maintaining communication with management and regulatory authorities if necessary.

Q: What experience do you have in developing GLP training programs?

Expected Answer: Should demonstrate experience in creating comprehensive training materials, implementing training programs, tracking staff competency, and ensuring ongoing compliance through regular assessments and updates.

Mid Level Questions

Q: What are the essential components of a GLP study?

Expected Answer: Should mention proper documentation, standard operating procedures (SOPs), quality control checks, proper data recording, and the importance of maintaining study integrity through proper sample handling and storage.

Q: How do you ensure proper documentation in a GLP environment?

Expected Answer: Should discuss the importance of detailed record-keeping, proper data entry procedures, maintaining chain of custody, and following documentation guidelines for corrections and modifications.

Junior Level Questions

Q: What does GLP mean and why is it important?

Expected Answer: Should be able to explain that GLP ensures quality and consistency in laboratory work, and why this is important for safety and reliability of test results.

Q: What are the basic requirements for working in a GLP environment?

Expected Answer: Should mention attention to detail, following procedures exactly, proper documentation practices, and the importance of asking questions when unsure.

Experience Level Indicators

Junior (0-2 years)

  • Basic laboratory techniques
  • Understanding of GLP principles
  • Basic documentation practices
  • Following standard operating procedures

Mid (2-5 years)

  • GLP compliance monitoring
  • Quality control procedures
  • Training junior staff
  • Writing and reviewing SOPs

Senior (5+ years)

  • GLP program management
  • Regulatory compliance oversight
  • Quality system development
  • Laboratory staff supervision

Red Flags to Watch For

  • No understanding of basic laboratory safety practices
  • Inability to explain documentation requirements
  • Lack of attention to detail in previous work
  • No experience with quality control procedures
  • Poor understanding of contamination prevention