GLP Training Specialist
Actalent, Raleigh, NC, United States
Job Title: GLP Training Specialist
We are seeking a GLP Training Specialist to develop and manage training programs within a regulated pharmaceutical environment. The specialist ensures compliance with Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and safety standards. This role involves supporting approximately 56 laboratory personnel across microbiology and chemistry functions through hands‑on, classroom, and on‑the‑floor training.
Responsibilities
Develop, deliver, and maintain GLP and GMP‑compliant training programs for laboratory personnel.
Ensure training content aligns with FDA, GLP, GMP, internal SOPs, and data integrity expectations.
Serve as a subject‑matter expert for GLP training requirements in a laboratory setting.
Conduct hands‑on and classroom training for microbiology and chemistry laboratory staff.
Deliver and reinforce training in 5S and laboratory housekeeping standards, basic GMP and GLP principles, laboratory safety, and core microbiology and chemistry practices.
Provide on‑the‑floor coaching to ensure correct application of procedures and good documentation practices.
Maintain accurate and audit‑ready training records in accordance with GLP/GMP requirements.
Support training matrix development and track initial, refresher, and remedial training.
Collaborate with QC, QA, EHS, and laboratory leadership to update training materials as procedures, regulations, or processes change.
Support onboarding and re‑training initiatives for new hires and existing staff.
Assist with investigations or CAPAs related to training deficiencies when required.
Essential Skills
Bachelor’s degree in Biology, Chemistry, Microbiology, or a related scientific discipline (or equivalent experience).
3 – 5 + years of experience in a GLP, GMP, or regulated pharmaceutical laboratory environment.
Demonstrated experience delivering laboratory training to scientific staff.
Working knowledge of microbiology and analytical chemistry laboratory operations.
Strong understanding of GLP, GMP, data integrity, and good documentation practices (GDP).
Ability to clearly communicate technical concepts to diverse laboratory audiences.
Excellent organizational, documentation, and presentation skills.
Comfortable training groups and providing one‑on‑one coaching in a lab setting.
Additional Skills & Qualifications
Prior experience in a training‑focused role within QC, QA, or laboratory operations.
Experience supporting regulatory inspections (FDA or equivalent).
Familiarity with electronic training systems (LMS) or training tracking tools.
Experience implementing or sustaining 5S programs in laboratory environments.
Work Environment This role is based on‑site in Wilson, working within normal business hours but with the flexibility to assist night shift training as needed. The work environment includes lab space within a DEA and GMP controlled setting.
Job Type & Location This is a Contract position based out of Raleigh, NC.
Pay and Benefits The pay range for this position is $40.00 – $50.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long‑term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Diversity, Equity & Inclusion
Hiring diverse talent
Maintaining an inclusive environment through persistent self‑reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal‑opportunity employer.
Application Deadline This position is anticipated to close on Mar 30, 2026.
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Responsibilities
Develop, deliver, and maintain GLP and GMP‑compliant training programs for laboratory personnel.
Ensure training content aligns with FDA, GLP, GMP, internal SOPs, and data integrity expectations.
Serve as a subject‑matter expert for GLP training requirements in a laboratory setting.
Conduct hands‑on and classroom training for microbiology and chemistry laboratory staff.
Deliver and reinforce training in 5S and laboratory housekeeping standards, basic GMP and GLP principles, laboratory safety, and core microbiology and chemistry practices.
Provide on‑the‑floor coaching to ensure correct application of procedures and good documentation practices.
Maintain accurate and audit‑ready training records in accordance with GLP/GMP requirements.
Support training matrix development and track initial, refresher, and remedial training.
Collaborate with QC, QA, EHS, and laboratory leadership to update training materials as procedures, regulations, or processes change.
Support onboarding and re‑training initiatives for new hires and existing staff.
Assist with investigations or CAPAs related to training deficiencies when required.
Essential Skills
Bachelor’s degree in Biology, Chemistry, Microbiology, or a related scientific discipline (or equivalent experience).
3 – 5 + years of experience in a GLP, GMP, or regulated pharmaceutical laboratory environment.
Demonstrated experience delivering laboratory training to scientific staff.
Working knowledge of microbiology and analytical chemistry laboratory operations.
Strong understanding of GLP, GMP, data integrity, and good documentation practices (GDP).
Ability to clearly communicate technical concepts to diverse laboratory audiences.
Excellent organizational, documentation, and presentation skills.
Comfortable training groups and providing one‑on‑one coaching in a lab setting.
Additional Skills & Qualifications
Prior experience in a training‑focused role within QC, QA, or laboratory operations.
Experience supporting regulatory inspections (FDA or equivalent).
Familiarity with electronic training systems (LMS) or training tracking tools.
Experience implementing or sustaining 5S programs in laboratory environments.
Work Environment This role is based on‑site in Wilson, working within normal business hours but with the flexibility to assist night shift training as needed. The work environment includes lab space within a DEA and GMP controlled setting.
Job Type & Location This is a Contract position based out of Raleigh, NC.
Pay and Benefits The pay range for this position is $40.00 – $50.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long‑term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Diversity, Equity & Inclusion
Hiring diverse talent
Maintaining an inclusive environment through persistent self‑reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal‑opportunity employer.
Application Deadline This position is anticipated to close on Mar 30, 2026.
#J-18808-Ljbffr