Jr. Validation Specialist

• →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.

• 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.

• Exposure to utilities, equipment qualification, or manufacturing processes.
• Internship or hands-on experience in validation or quality environments.
• Experience with documentation practices in regulated industries.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.