Life Sciences Validation Engineer – Entry Level

Barry-Wehmiller Companies Inc.

Carmel (IN)

On-site

USD 75,000 - 90,000

Full time

14 days+

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Job summary

Barry-Wehmillher Companies Inc. seeks a highly organized validation engineer to ensure pharmaceutical and life sciences equipment meets regulatory standards. You will develop protocols, execute tests, and document results across projects.

Join a collaborative team in Carmel, Indiana, supporting FAT/SAT/IQ/OQ activities and contributing to quality management and site validation efforts.

Qualifications

Bachelor of Science in bioengineering, biomedical engineering, chemical engineering, or a related technical degree.
Experience related to validation, quality, pharmaceutical manufacturing, medical devices, automation, utilities, facilities, or regulated environments.
Proficiency using Microsoft Office and ability to prepare clear technical documentation.
Ability to travel for project requirements, including installation and start-up activities, client and company meetings.

Responsibilities

Support validation and regulatory compliance activities for pharmaceutical, medical device, and other life sciences projects.
Develop and execute protocols, test plans, investigate issues, and document results.
Prepare FAT, SAT, IQ, and OQ documentation for equipment and automated systems.
Assist with development and execution of quality management system procedures and related compliance documentation.
Coordinate with clients, vendors, engineers, and project teams to support validation planning and execution.
Support installation, start-up, commissioning, and site-based validation activities.