Senior Validation Specialist

6 days ago


North East, United Kingdom AMARIS GROUP SA Full time

**About the Role:**

We are seeking a skilled Validation Specialist to join our quality and validation team for a significant project in the pharmaceutical industry. The position involves working on facility extension, new equipment installation, and production scale-up.

**Key Responsibilities:

  • Lead and execute commissioning, qualification, and validation (CQV) activities for equipment and systems.
  • Develop, review, and approve validation protocols (IQ/OQ/PQ) and related documentation.
  • Ensure compliance with FDA regulations and GMP standards across all validation processes.

**Requirements:**

  • Experience: 5–10 years of experience in CQV roles, with a minimum of 5 years in equipment validation and qualification in the pharmaceutical industry.
  • Knowledge: Strong understanding of FDA regulations, GMP, and validation best practices.

**Estimated Salary:** $120,000 - $180,000 per annum.


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