Senior Facilities Engineer: Sterile GMP Equipment

Afton Scientific. LLC

Charlottesville (VA)

On-site

USD 50,000 - 69,000

Full time

14 days+

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Job summary

Afton Scientific is seeking an experienced Senior Facilities Engineer to join our facilities team in Virginia. This role provides hands-on technical support for pharmaceutical process equipment, troubleshoots issues, and strengthens preventive maintenance practices to sustain sterile manufacturing operations.

Collaborate with Manufacturing, Engineering, MS&T, EHS, and other teams to manage equipment reliability, documentation, and process improvements in a compliant, fast-paced environment.

Qualifications

  • Six years of maintenance experience on manufacturing equipment or an Associate degree or higher in a related field.
  • Experience in a sterile fill-finish manufacturing environment.
  • Strong understanding of GMP standards and regulatory requirements.
  • Ability to work independently while following procedures.

Responsibilities

  • Serve as a technical resource to production teams for process equipment.
  • Act as first responder for equipment malfunctions and drive timely troubleshooting.
  • Support equipment such as fill lines, isolators, autoclaves, and related machinery.
  • Collaborate with owners, engineers, vendors, and other resources to diagnose and resolve issues.
  • Support preventive maintenance and calibration activities.
  • Develop and update preventive maintenance instructions and manage inventories of critical spare parts.
  • Complete work orders and GMP records accurately and on time.
  • Identify recurring equipment issues and work with teams on sustainable solutions.
  • Assist training of Manufacturing personnel on process equipment.

Skills

Troubleshooting
Maintenance
GMP knowledge
CMMS
Communication

Education

Associate degree in Engineering

Tools

CMMS

Job description

Afton Scientific is seeking an experienced Senior Facilities Engineer to join our facilities team in Virginia. This role provides hands-on technical support for pharmaceutical process equipment, troubleshoots issues, and strengthens preventive maintenance practices to sustain sterile manufacturing operations.

Collaborate with Manufacturing, Engineering, MS&T, EHS, and other teams to manage equipment reliability, documentation, and process improvements in a compliant, fast-paced environment.

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