GMP Program Coordinator | Compliance & Training Lead

Pacific West Site Services, Inc.; New Albany (OH); On-site; USD 23,000 - 25,000; Full time

Benefits offered by this job

Benefits package

Job summary

Pacific West Site Services, Inc. is seeking a GMP Coordinator to coordinate and manage project tasks within the GMP program, ensuring delivery on time and within budget. The role requires attention to safety, quality documentation, and effective communication with the team and customers.

The successful candidate will support GMP managers, maintain logs and SOPs, and assist with training and onboarding. Local Ohio operations in the New Albany area may involve shift coordination and routine GMP

Qualifications

• High school diploma or GED preferred.
• 6 months to 1 year of related experience preferred.
• CPR/AED/First Aid certification a plus.
• May be required to have a valid driver’s license.
• Completed all safety and task training certifications.
• Forklift certification may be required.

Responsibilities

• Coordinate and manage GMP program tasks to meet budget and timelines.
• Comply with safety rules, policies, and procedures.
• Communicate professionally with lead, supervisor, coworkers, managers, and customers.
• Maintain clear and accurate GMP documents and procedures.
• Review logbooks, log sheets, and GDP documents for accuracy.
• Assist with training and qualification of new hires.

Skills

Verbal communication

Safety awareness

Team coordination

Documentation

Education

High school diploma or GED

Tools

CMMS

Job description

Pacific West Site Services, Inc. is seeking a GMP Coordinator to coordinate and manage project tasks within the GMP program, ensuring delivery on time and within budget. The role requires attention to safety, quality documentation, and effective communication with the team and customers.

The successful candidate will support GMP managers, maintain logs and SOPs, and assist with training and onboarding. Local Ohio operations in the New Albany area may involve shift coordination and routine GMP