Senior Validation Manager: GMP Compliance & Team Leadership

Hyper Recruitment Solutions Ltd

England

A distancia

GBP 75.000 - 100.000

Jornada completa

Hace 2 días
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Descripción de la vacante

Hyper Recruitment Solutions Ltd in Kent, United Kingdom is seeking a Validation Manager to lead a high-performing validation team within a GMP-regulated pharmaceutical manufacturing environment.

This senior role controls validation across facilities, equipment and processes, develops Validation Master Plans, SOPs and protocols, and ensures regulatory readiness in line with EudraLex Volume 4 Annex 11 and 15, collaborating with Quality, Engineering and Operations teams.

Formación

  • Degree-level qualification in Chemistry, Biology, Engineering or related scientific discipline.
  • Minimum of 10 years' experience in validation and GMP-regulated pharmaceutical manufacturing.
  • Proven experience leading and developing validation teams.
  • Experience authoring validation protocols and Validation Master Plans (VMPs).

Responsabilidades

  • Coordinate and perform validation project activities for facilities, equipment, systems, and processes in compliance with GMP requirements.
  • Lead, develop, and mentor the validation team including recruitment, training, and performance management.
  • Establish and maintain validation procedures, Validation Master Plans (VMPs), SOPs, and best practices.
  • Prepare, execute, and review validation protocols and reports in line with regulatory and company requirements.
  • Review, update, and maintain validation documentation to evolving regulatory expectations.

Conocimientos

Team leadership
Validation expertise
GMP knowledge
Regulatory awareness

Educación

Bachelor's degree in Chemistry/ Biology/ Engineering

Descripción del empleo

Hyper Recruitment Solutions Ltd in Kent, United Kingdom is seeking a Validation Manager to lead a high-performing validation team within a GMP-regulated pharmaceutical manufacturing environment.

This senior role controls validation across facilities, equipment and processes, develops Validation Master Plans, SOPs and protocols, and ensures regulatory readiness in line with EudraLex Volume 4 Annex 11 and 15, collaborating with Quality, Engineering and Operations teams.

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