Equipment Qualification Engineer

ManpowerGroup Global, Inc.; Swiftwater (Monroe County); On-site; USD 85,000 - 120,000; Full time

Job summary

ManpowerGroup Global, Inc. is seeking an Equipment Qualification Engineer in Swiftwater, PA to support GMP validation efforts within Quality Assurance and Engineering.

You will lead requalification activities, review protocols, and execute IQ/OQ/PQ tasks to ensure equipment performance and documentation integrity. You will collaborate with multi-disciplinary teams on CQV activities across production and utility systems, manage deviations and CAPA linked to qualification projects, and contribute

Qualifications

• Experience in GMP validation activities.
• Knowledge of IQ/OQ/PQ processes and validation protocols.
• Background in Engineering, Utilities & Facilities management.

Responsibilities

• Lead and execute equipment requalification activities to ensure GMP compliance.
• Prepare and review qualification protocols and reports to maintain documentation integrity.
• Perform IQ/OQ/PQ activities to validate equipment performance and functionality.
• Support CQV execution across production and utility systems.
• Manage deviations and CAPA linked to qualification activities.

Skills

Equipment requalification

GMP validation

IQ/OQ/PQ processes

CAPA management

Lifecycle management

Education

Engineering degree

Job description

Our client is seeking a Equipment Qualification Engineer to join their team. As a Equipment Qualification Engineer, you will be part of the Quality Assurance and Engineering departments supporting equipment validation and GMP compliance initiatives.

Job Title: Equipment Qualification Engineer

Location:Swiftwater, PA

What's the Job?

• Lead and execute equipment requalification activities to ensure compliance with GMP standards.
• Prepare and review qualification protocols and reports to maintain documentation integrity.
• Perform IQ/OQ/PQ activities to validate equipment performance and functionality.
• Support Commissioning, Qualification, and Validation (CQV) execution across production and utility systems.
• Manage deviations and CAPA linked to qualification activities to continuously improve processes.

What's Needed?

• Experience in Equipment Requalification and GMP validation activities.
• Knowledge of IQ/OQ/PQ processes and validation protocols.
• Background in Engineering, Utilities, & Facilities management.
• Strong understanding of Equipment Lifecycle Management.
• Ability to manage deviations and CAPA effectively.

What's in it for me?

• Opportunity to work on impactful validation projects in a dynamic environment.
• Collaborate with multidisciplinary teams to ensure GMP compliance.
• Enhance your expertise in equipment qualification and validation processes.
• Gain valuable experience supporting remediation and requalification programs.
• Join a company committed to quality and continuous improvement.