Quality Manager

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Overview

CK Group are recruiting for a Quality Manager to join a Pharmaceutical Services Company in Central Belt Scotland. This is a permanent role with Mon-Fri daytime working hours and hybrid working available.

Responsibilities

  • Maintain, develop, and continuously improve the QMS in line with GMP, GLP, ISO 17025, and client requirements.
  • Oversee document control, ensuring SOPs, policies, and records remain current, accurate, and reflective of best practice.
  • Lead internal audits, management reviews, and risk assessments, embedding quality into all aspects of our work.
  • Manage and ensure timely closure of deviations, non-conformances, CAPAs, and change controls.
  • Act as lead contact for MHRA, FDA, and other regulatory inspections, as well as client audits.
  • Support client projects and technical discussions to ensure full alignment with quality expectations.
  • Lead and mentor the Quality team, fostering accountability, ownership, and professional development.

Your Background

  • Essential:
  • Degree in a relevant life sciences discipline (e.g., Biology, Chemistry, Pharmaceutical Sciences).
  • Substantial quality management experience in a contract laboratory, CRO, or pharmaceutical environment.
  • Strong knowledge of GMP, GLP, ISO 17025, and other applicable standards in pharmaceutical and life sciences sectors.
  • Track record of successful regulatory inspections and client audit management.
  • Proven experience of leading and enhancing QMS systems.
  • Line management or leadership experience.
  • Desirable:
  • Familiarity with electronic QMS platforms (advantageous).

Apply

It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

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Location:
City Of Edinburgh, Scotland, United Kingdom
Salary:
£80,000 - £100,000
Job Type:
FullTime
Category:
IT & Technology

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