Validation Engineer - Contract
Disher•Grand Rapids, MI
•Hybrid
About The Position
DISHER is seeking an experienced Validation Engineer to support a customer team with engineering work to develop and execute IQ/OQ/PQ process validation. The engineer will help develop a Validation Master Plan (VMP), create protocols and supporting documents, and execute process validation. This is a hybrid contract position, with onsite work in Grand Rapids as needed. The expected duration is eight weeks, with potential to extend. The role involves a 40-hour workweek.
Requirements
- Bachelor's degree in Quality Engineering, Validation Engineering, or a related engineering field.
- Experience developing Validation Master Plans (VMPs).
- Experience developing validation processes (IQ/OQ/PQ).
- Ability to document protocols, process validation, quality plans, work instructions, and related materials.
- Ability to work onsite in Grand Rapids as needed.
Nice To Haves
- 1–5 years of medical device experience preferred.
Responsibilities
- Develop a Validation Master Plan (VMP).
- Develop protocols and supporting documents, and execute process validation (IQ, OQ, PQ).
- Prepare documentation including protocols, IQ/OQ/PQ materials, quality plans, work instructions, label masters, quality inspection documentation, and testing documentation.
- Work onsite in Grand Rapids as needed.
