GLP

Term from Pharmaceutical Services industry explained for recruiters

GLP (Good Laboratory Practice) is a set of rules and standards that ensure laboratory work is done safely and accurately, especially in pharmaceutical and medical research. Think of it like a recipe book that scientists must follow to make sure their work is reliable and can be trusted. These standards are particularly important when testing new medicines or conducting safety studies, as the results will be reviewed by government agencies like the FDA. When you see GLP mentioned in a resume, it means the person knows how to work according to these strict quality standards.

Examples in Resumes

Conducted safety studies following GLP standards in preclinical research

Managed laboratory operations in compliance with GLP and Good Laboratory Practice guidelines

Led team of technicians in GLP-certified facility for drug development studies

Typical job title: "GLP Laboratory Scientists"

Also try searching for:

Laboratory Scientist Research Associate Lab Manager Quality Assurance Specialist Preclinical Research Scientist GLP Study Director Laboratory Technician

Example Interview Questions

Senior Level Questions

Q: How would you handle a significant GLP compliance deviation in your lab?

Expected Answer: A senior scientist should explain the process of documenting the deviation, assessing its impact on study integrity, implementing corrective actions, and communicating with regulatory authorities if necessary.

Q: How would you set up a new GLP-compliant laboratory from scratch?

Expected Answer: Should discuss establishing SOPs, training programs, documentation systems, quality control measures, and working with quality assurance to ensure all systems meet GLP requirements.

Mid Level Questions

Q: What are the key elements of GLP documentation?

Expected Answer: Should mention proper record-keeping practices, importance of dated signatures, handling corrections, maintaining study protocols, and writing final reports.

Q: How do you ensure data integrity in GLP studies?

Expected Answer: Should explain the importance of proper data recording, backup procedures, audit trails, and systems for preventing unauthorized changes to data.

Junior Level Questions

Q: What are the basic principles of GLP?

Expected Answer: Should be able to explain the fundamental concepts of proper documentation, following protocols, equipment maintenance, and the importance of accuracy in recording data.

Q: How do you maintain a laboratory notebook according to GLP standards?

Expected Answer: Should describe proper documentation practices like using permanent ink, dating entries, avoiding blank spaces, and properly recording corrections.

Experience Level Indicators

Junior (0-2 years)

  • Basic laboratory techniques
  • Understanding of GLP principles
  • Following Standard Operating Procedures
  • Basic documentation practices

Mid (2-5 years)

  • Study protocol implementation
  • Data analysis and reporting
  • Equipment calibration and maintenance
  • Training junior staff

Senior (5+ years)

  • Study design and oversight
  • Quality system management
  • Regulatory compliance
  • Program/facility management

Red Flags to Watch For

  • No understanding of basic documentation requirements
  • Lack of attention to detail in previous work
  • Unable to explain quality control measures
  • No experience with regulatory compliance
  • Poor understanding of data integrity principles

Related Terms