Validation Specialist

4 days ago


Reston, Virginia, United States Hyper Recruitment Solutions Full time
Validation Engineer Job Description

We are seeking a highly skilled Validation Engineer to join our team at Hyper Recruitment Solutions.

About the Role:

This is an exciting opportunity to work as a Validation Engineer in the Pharma and Life Sciences industries. As a Validation Engineer, you will be responsible for validating complex automated manufacturing equipment, writing validation protocols (IQ/OQ), and presenting the results to end customer project teams.

Key Responsibilities:

  • Validating large complex automated manufacturing equipment, including solid dosage, capsules, tablet pressers, fluid beds, granulates, and spin blenders.
  • Writing validation documents for large complex systems, including IQ's up to 200 pages and OQ's up to 700 pages.
  • Presenting the validation results to end customer project teams, including QA, validation, project management, and other stakeholders.
  • Traveling to customers' sites, typically based around CT and MI, for approximately 25-30% of the time.

Requirements:

  • Experience in a Pharma/Biotech/Life Science/GMP environment.
  • Degree in a relevant engineering field.
  • Must have worked with complex automated manufacturing equipment.
  • Must have experience in document writing IQ/OQ's.
  • Must be comfortable traveling to customers' sites and spending a week on site.

What We Offer:

We offer a competitive salary, bonus, and benefits package, as well as opportunities for progression and development within the organization.

How to Apply:

If you have the relevant skills and experience, please respond with an application to this advert or directly to us.


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