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QA Specialist

SRG
Posted 3 days ago, valid for 6 days
Location

Glasgow, City of Glasgow G2 5LA, Scotland

Salary

£28,000 - £33,600 per year

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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 experience in Quality Assurance within a GMP environment.
  • The position is initially for 12 months with a high possibility of extension, offering excellent benefits and opportunities for growth.
  • Key responsibilities include performing batch reviews, authoring SOPs, and supporting supplier audits and regulatory inspections.
  • Candidates should possess a degree in a relevant field and experience with Quality Management Systems, along with strong communication skills.
  • The salary for this role is competitive, reflecting the experience and expertise required.

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.

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

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

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