Quality Assurance Specialist (Validation)

at  Almac Group

KEY REQUIREMENTS

Applicants must have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time, permanent employment in the UK

DESIRABLE CRITERIA

• Masters or Bsc in a scientific subject (or equivalent)
• Previous experience in writing and producing detailed reports
• Direct experience in the manufacture of solid oral dosage products
• Quality Risk Management
• Root Cause Analysis
• Lean six sigma trained
  Please see attached job description for further details of criteria.

THE ROLE

A typical day for a Quality Assurance Specialist in Almac Pharma Services is far from typical. The role is varied and dynamic. You will play a pivotal role in supporting QA activities with a focus on qualification and validation in line with Almac Pharma Services global standards. Responsibilities include QA oversight of facility, equipment, and utility qualification, as well as approval of various QA documentation like SOPs, Change Controls, Deviations, and CAPAs.
As the post holder, you’ll be involved in reviewing and approving validation lifecycle documentation, conducting Data Integrity risk assessments, and acting as a QA Validation Subject Matter Expert for planned and unplanned changes. Keeping up-to-date with regulatory requirements and industry expectations is key, along with providing crucial support for site compliance to ensure quality assurance.
Please see attached job description for further details.