Disher

Product development, talent, and business consulting

Validation Engineer

Validation, Compliance & Quality SystemsPosted on Nov 9

ContractGrand Rapids, MI, USANo salary listed

About the Job

Requirements

A bachelor's degree in Quality Engineering, Validation Engineering, or a related Engineering degree is required.
Experience developing Validation Master Plans (VMPs) is required.
Experience developing process validation (IQ/OQ/PQ) is required.
Ability to document protocols, process validation, quality plans, work instructions, and related materials is required.
Ability to work onsite in Grand Rapids as needed is required.

Responsibilities

Develop a Validation Master Plan (VMP).
Develop protocols and supporting documents, and execute process validation (IQ/OQ/PQ).
Complete documentation work involving protocols, IQ/OQ/PQ, quality plans, work instructions, label masters, quality inspection, and testing.
Work a 40-hour week for 8 weeks and go onsite in Grand Rapids as needed.

Desired Qualifications

One to five years of medical device experience is preferred.

Validation Engineer- Contract

DISHER is seeking an experienced Validation Engineer to support a customer team providing engineering support to develop and execute IQ/OQ/PQ process validation. Engineer will help develop a Validation Master Plan (VMP), develop protocols and supporting documents, and execute process validation. This is a hybrid position with onsite in Grand Rapids as needed. Duration expected to last 8 weeks with potential to extend.

What it's like to work here

Make a positive difference! It’s why we exist. We are always looking for teammates who are eager to use their diverse set of talents with our customers, coworkers, and communities. We want to leave this world better than we found it.

What you will get to do:

Develop Validation Master Plan (VMP)
Develop Protocol and supporting documents and execute process validation (IQ, OQ, PQ)
Documentation work: protocol, IQ/OQ/PQ, quality plan, work instructions, label masters, quality inspection, and texting
Work 40 hour week for 8 weeks and go onsite in Grand Rapids as needed

What will make you successful:

Bachelor's degree in Quality Engineering, Validation Engineering, or a related Engineering degree
Experience developing VMP's
Experience developing validation process (IQ/OQ/PQ)
Ability to document protocols, Process validation, quality plan, work instructions, etc.
Work onsite in Grand Rapids as needed
1-5 years of medical device experienced preferred

About the Company

Disher

Product development, talent, and business consulting

Disher provides product development, talent recruitment, and business consulting services to help large organizations and inventors bring products to market. Its team collaborates with clients to discover, design, engineer, and manufacture products and services, while also sourcing and placing specialized talent and addressing broader business needs. Serving industries such as automotive, office furniture, energy, consumer, agribusiness, industrial, and medical, Disher leverages offices in Michigan and Indiana to support clients locally and nationwide. Its goal is to improve client performance and profitability by turning ideas into market-ready solutions and building teams and processes that sustain growth.

Company size: 51-200
Company stage: Not listed
Total funding: Not listed
Headquarters: Zeeland, MI
Founded: 2000

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