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Validation Engineer - Contract

πŸ•’ yesterday
Process ValidationIQ/OQ/PQValidation Master Plan (vmp)Protocol Development
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πŸ“œ Description

  • Create validation protocols and supporting documents, then execute IQ/OQ/PQ process validation.
  • Prepare quality plans, work instructions, label masters, and quality inspection documentation.
  • Support documentation and testing activities.

πŸ› οΈ Requirements

  • Bachelor’s degree in Quality Engineering, Validation Engineering, or a related engineering field.
  • Experience developing Validation Master Plans.
  • Experience developing and executing IQ/OQ/PQ validation processes.
  • Ability to document protocols, process validation, quality plans, and work instructions.
  • 1–5 years of medical device experience preferred.
  • Develop a Validation Master Plan (VMP).
Full job description

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
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