Junior Validation Specialist - IQ/OQ/PQ Execution (GMP)

Validation & Engineering Group, Inc.

Carolina (PR)

On-site

USD 42,000 - 65,000

Full time

14 days+
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Job summary

Validation & Engineering Group, Inc. in the United States is seeking a motivated Junior Validation Specialist to support validation and qualification activities in a regulated environment.

You will participate in testing, documentation, and field execution under supervision. The role emphasizes attention to detail, coordination with Engineering, Quality, and Operations, and adherence to GMP and company procedures.

Qualifications

  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • 1–3 years of experience in validation, CQV, or related technical role in a regulated industry.
  • Basic understanding of GMP and regulatory requirements.
  • Familiarity with validation lifecycle concepts (IQ/OQ/PQ).
  • Strong attention to detail and organizational skills.
  • Good communication and teamwork abilities.

Responsibilities

  • Support execution of validation and qualification protocols (IQ, OQ, PQ).
  • Assist with testing activities, data collection, and data logging.
  • Perform field verification of systems and equipment under supervision.
  • Assist in the preparation and review of validation documentation, including protocols and reports.
  • Ensure all activities are performed in compliance with GMP and company procedures.
  • Support deviation investigations, CAPAs, and documentation updates as needed.
  • Collaborate with cross-functional teams including Engineering, Quality, and Operations.

Skills

Attention to detail
Communication skills
Teamwork

Education

Bachelor’s degree in Engineering/Life Sciences or related field

Job description

Validation & Engineering Group, Inc. in the United States is seeking a motivated Junior Validation Specialist to support validation and qualification activities in a regulated environment.

You will participate in testing, documentation, and field execution under supervision. The role emphasizes attention to detail, coordination with Engineering, Quality, and Operations, and adherence to GMP and company procedures.

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