Junior Validation Specialist (IQ/OQ/PQ)

Sentry BioPharma Services Inc; Maple Ridge (IN); On-site; USD 60,000 - 75,000; Full time

Job summary

Sentry BioPharma Services Inc. is seeking a detail-oriented Validation Associate I to join our team in Indiana.

You will execute IQ/OQ/PQ validation activities and support qualification efforts to ensure equipment and processes meet quality and regulatory standards. Join a collaborative environment where you’ll generate validation reports, analyze data, and drive continuous improvement while adhering to cGMP, FDA requirements, and scheduled timelines.

Qualifications

• Bachelor’s degree in Life Sciences, Engineering, or a related field.
• 1–3 years of validation/gmp experience preferred.
• Knowledge of cGMP and FDA regulations.
• Attention to detail and strong organizational skills.
• Excellent problem-solving and troubleshooting abilities.
• Effective written and verbal communication.
• Ability to work independently and in a team.
• Willingness to travel to multiple Sentry locations.

Responsibilities

• Execute IQ, OQ, and PQ validation protocols.
• Generate and review validation/qualification reports.
• Provide support and troubleshooting for all validated/qualified equipment.
• Identify opportunities for process improvements and assist in implementing effective solutions.
• Ensure all validation activities are conducted in compliance with cGMP, FDA, and other applicable regulatory requirements.
• Collaborate with cross-functional teams to support validation projects and ensure timely completion.

Skills

Attention to detail

Problem solving

Communication skills

Teamwork

Education

Bachelor’s degree in Life Sciences/Engineering

Job description

Sentry BioPharma Services Inc. is seeking a detail-oriented Validation Associate I to join our team in Indiana.

You will execute IQ/OQ/PQ validation activities and support qualification efforts to ensure equipment and processes meet quality and regulatory standards. Join a collaborative environment where you’ll generate validation reports, analyze data, and drive continuous improvement while adhering to cGMP, FDA requirements, and scheduled timelines.