Senior Quality Manager

Cranleigh STEM

Dartford

Hybrid

GBP 80,000 - 85,000

Full time

6 days ago
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Benefits offered by this job

Performance-related bonus
Hybrid working after probation
Private medical and dental cover
Life assurance – 4x basic salary
Pension with employer contributions
25 days' holiday + bank holidays

Job summary

Initially site-based with hybrid working after probation and flexible hours, the role offers £80,000–£85,000 plus a bonus as part of a comprehensive benefits package.

Qualifications

  • Pharmaceutical industry knowledge essential
  • Extensive QA leadership in a regulated manufacturing environment
  • Strong understanding of GMP, ISO 9001, QMS
  • Experience with EXCiPACT and IPEC guidelines
  • Experience overseeing raw material and finished product QA
  • Proven ability to lead multidisciplinary quality teams
  • Auditing, root-cause analysis and continuous improvement experience
  • Commercial awareness and ability to influence senior stakeholders

Responsibilities

  • Lead and continuously improve the site's Quality Management System (QMS)
  • Ensure compliance with GMP, ISO 9001, EXCiPACT and IPEC guidelines
  • Oversee raw material and finished product QA including release decisions
  • Lead and develop multidisciplinary quality teams
  • Manage quality audits, regulatory compliance and customer quality requirements
  • Oversee change control, CAPA, risk management and controlled documentation
  • Drive continuous improvement and strengthen quality culture across the site
  • Collaborate with senior leadership and global teams to deliver strategic quality objectives

Job description

Senior Quality Manager

  • Location: Dartford, Kent

  • Salary: £80,000 – £85,000 + Bonus

  • Contract: Full-Time, Permanent

  • Working Arrangement: Initially Site-Based | Hybrid Working After Probation | Flexible Hours

We’re working exclusively with an international pharmaceutical organisation to recruit a Senior Quality Manager.

This is a senior leadership opportunity, taking overall responsibility for the site's Quality Assurance function, including the Quality Management System, raw materials, finished goods and auditing teams.

You’ll play a key role in driving quality strategy, regulatory compliance and continuous improvement, whilst developing high-performing teams and collaborating with senior stakeholders across the business.

Key Responsibilities:
  • Lead and continually improve the site's Quality Management System (QMS)

  • Ensure compliance with GMP, ISO 9001, EXCiPACT and IPEC guidelines

  • Oversee raw material and finished product quality assurance, including product release decisions

  • Lead, develop and manage multidisciplinary quality teams

  • Manage quality audits, regulatory compliance and customer quality requirements

  • Oversee change control, CAPA, quality risk management and controlled documentation

  • Drive continuous improvement and strengthen quality culture across the site

  • Collaborate with senior leadership and global teams to deliver strategic quality objectives

About You:
  • Pharmaceutical industry knowledge is essential

  • Extensive Quality Assurance leadership experience within a regulated manufacturing environment

  • Strong understanding of GMP, ISO 9001 and Quality Management Systems

  • Knowledge of EXCiPACT and IPEC guidelines

  • Experience overseeing raw material and finished product quality activities

  • Proven ability to lead and develop multidisciplinary quality teams

  • Strong audit management, root cause analysis and continuous improvement experience

  • Commercial awareness and confidence influencing senior stakeholders

What's on Offer?
  • £80,000 – £85,000 basic salary

  • Performance-related bonus scheme

  • 25 days' holiday + bank holidays, with the option to purchase additional leave

  • Pension with double-matched contributions up to 10%

  • Private medical and dental cover

  • Life assurance – 4x basic salary

  • Income protection insurance

  • Flexible working hours

  • Hybrid working following successful completion of probation

  • Training and development opportunities

The role will initially be site-based during probation, with hybrid working available once established.

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