QA Specialist

 
 
  • Location: Glasgow

  • Job Type: Contract/Temporary

  • Reference: BBBH165753_1754059659

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

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