Validation Specialist

4 days ago


New York, New York, United States Hyper Recruitment Solutions Full time
Validation Engineer

Hyper Recruitment Solutions is seeking a skilled Validation Engineer to join our client's US Validation Department. As a key member of the team, you will be responsible for writing validation protocols (IQ/OQ) and validating large complex automated manufacturing equipment in the Pharma & Life Sciences industries.

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 validation results to end customer project teams, including QA, validation, project management, and other stakeholders.
  • Traveling to customer sites (25-30% of the time) to conduct validation activities.

Requirements:

  • Experience in Pharma/Biotech/Life Science/GMP environment.
  • Degree in a relevant engineering field.
  • Proven experience with large complex automated manufacturing equipment.
  • Strong document writing skills, including IQ/OQ's.
  • Comfortable traveling to customer sites and spending time on site.

What We Offer:

A competitive salary, bonus, and benefits package, as well as opportunities for career growth and development within a global leader in the CDMO/OEM industry.


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