Junior Validation Specialist — IQ/OQ/PQ, GMP Focus

Validation & Engineering Group; Carolina (PR); On-site; USD 52,000 - 78,000; Full time

Job summary

Validation & Engineering Group, Inc. in the United States is seeking a Junior Validation Specialist with 1–3 years of experience to support validation activities in a regulated environment. The role involves testing, documentation, and field execution under supervision.

The position focuses on GMP compliance, IQ/OQ/PQ work, and teamwork with Engineering, Quality, and Operations to deliver compliant results across pharma, biotech, and medical devices projects.

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 (pharma, biotech, or medical devices).
• 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

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 Junior Validation Specialist with 1–3 years of experience to support validation activities in a regulated environment. The role involves testing, documentation, and field execution under supervision.

The position focuses on GMP compliance, IQ/OQ/PQ work, and teamwork with Engineering, Quality, and Operations to deliver compliant results across pharma, biotech, and medical devices projects.