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QA Specialist

SRG
Posted 16 hours ago, valid for 17 days
Location

Glasgow, City of Glasgow G2 5LA, Scotland

Salary

£25,000 - £30,000 per annum

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Contract type

Full Time

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Sonic Summary

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  • SRG is seeking a QA Specialist for a global pharmaceutical company, requiring several years of Quality Assurance experience in a GMP environment.
  • The role involves performing batch reviews, authoring SOPs, and ensuring compliance with GMP regulations.
  • Candidates should have a degree in a relevant field and experience with Quality Management Systems and external audits.
  • The position offers a competitive salary and an excellent benefits package, along with opportunities for growth and development.
  • Strong organizational and communication skills are essential for success in this role.

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.

The Role:

  • 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

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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