More jobs:
QA Specialist
Job in
Glasgow, Glasgow City Area, G1, Scotland, UK
Listed on 2026-02-28
Listing for:
SRG
Full Time
position Listed on 2026-02-28
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Job Description & How to Apply Below
Overview
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.
Responsibilities- 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
- 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, Carbon
60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
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