Junior Validation Specialist: Grow in GMP & CQV (Pharma)

Veg Group; Puerto Rico; On-site; USD 54,000 - 78,000; Full time

Job summary

Validation & Engineering Group, Inc. in the United States, Puerto Rico area is seeking a Junior Validation Specialist with 1–3 years of experience to support validation activities in a regulated environment.

You will assist with testing, documentation, and field execution under supervision to grow your career in validation. Collaborate with Engineering, Quality, and Operations teams to ensure GMP compliance.

Qualifications

• 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.

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.

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, Puerto Rico area is seeking a Junior Validation Specialist with 1–3 years of experience to support validation activities in a regulated environment.

You will assist with testing, documentation, and field execution under supervision to grow your career in validation. Collaborate with Engineering, Quality, and Operations teams to ensure GMP compliance.