Associate Validation Engineer

Transcat•Colombus, OH

11d•Hybrid

About The Position

Transcat is seeking a full-time Associate Validation Engineer to work closely with clients to address their Validation needs. This position is ideal for candidates located in Ohio, preferably near Dayton, Ohio. The role requires up to 75% travel to support various client sites and reports directly to the Validation Manager. Transcat is a dynamic, innovative, and growing company recognized as a leading calibration and compliance services provider. With over 1,000 employees, we deliver on our promise to customers in vital industries like life sciences, aerospace, defense, energy, and utilities. We offer a rewarding and challenging work environment with flexibility, exposure to diverse projects, covered travel expenses, a values-based culture, and opportunities for training and career advancement. We also provide competitive compensation and benefits.

Requirements

An associate’s degree or 2 years of work experience.
Strong troubleshooting and problem-solving skills.
Strong attention to detail.
Strong interpersonal skills: ensuring the ability to interact with clients and peers in a professional manner.
Proficient with operating Windows computers, MS Office, and ability to quickly learn new software.
Ability to work in a fast-paced environment while supporting multiple and changing priorities.
Ability to work independently and work in collaborative teams.
Ability to work in different temperature environments- including but not limited to heat and freezers of -40 degrees.
Ability to lift, push, pull, and carry up to 55 pounds.
A valid Driver’s license.
Flexibility to travel up to 75% of the time.

Nice To Haves

Bachelor's or Associate degree in a STEM field or trade certification in mechanical, electrical, instrumentation, industrial technology, or a related discipline
Experience supporting pharmaceutical, biotechnology, or other regulated manufacturing environments

Responsibilities

Execute qualifications for client’s laboratory equipment and/or storage facilities in support of GMP/FDA requirements by executing PM, IQ, OQ, and PQ protocols.
Follow Good Laboratory/Documentation Practices.
Troubleshoot electrical, mechanical, and computerized software/ systems.
Establish and maintain close communication with assigned clients to ensure superior customer satisfaction.
Other duties as required.