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QA Specialist

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SRG

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Location:
United Kingdom , Glasgow

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Category:
Pharmacy

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

SRG are working with a global name in the pharmaceutical industry to help them find a QA Specialist to join their team. If you have Quality Assurance (QA) experience from a GMP environment then this could be a great next step for you. The company offer an excellent benefits package and scope for growth and development. This role is for an initial 12 months with a strong likelihood of being extended from there.

Job Responsibility:

  • Perform batch reviews within required timelines
  • Author and review SOPs
  • Document and report all work in adherence with GMP and departmental procedures
  • Review change controls and provide feedback / corrections to authors and escalate concerns to the Quality Manager/Head of Quality where necessary
  • Raise, approve and review CAPAs
  • Represent the QA team for improvement projects and with clients and internal teams
  • Assist in the performance of supplier audits, supporting the Lead Auditor
  • Acts as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and information
  • Conducts self-inspections / audits to ensure compliance with Quality Management System procedures and GMP regulations
  • Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management
  • Carries out site internal audits and identifies areas of GMP improvement during their daily duties
  • Carries out training for QMS activities as defined by line management

Requirements:

  • Degree in a relevant scientific, engineering or business discipline and/or relevant industry experience
  • Several years' experience within Quality Assurance working to GMP guidelines
  • Experience of working within a Quality Management System e.g. completing or reviewing QMS documentation (SOPs/Deviations /Investigations /CAPA)
  • Experience of preparing and assisting in external audits with regulatory bodies such as FDA and MHRA
  • Organised and attention to detail
  • Strong communication skills across all levels
What we offer:
  • Excellent benefits package
  • Scope for growth and development

Additional Information:

Job Posted:
January 25, 2026

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