Quality Assurance Specialist

Meet Life Sciences Ltd.

Greater London

Híbrido

GBP 42.000 - 60.000

Jornada completa

hace 37 horas
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Descripción de la vacante

Meet Life Sciences Ltd. is seeking a Quality Assurance Specialist to strengthen the QMS and ensure GDP compliance. The role covers deviation handling, CAPAs, change controls, investigations, and risk assessments in a broad quality environment.

You will review SOPs, manage documentation systems, support audits, recalls, and regulatory activities while promoting a culture of quality across the business. This is a 12-14 month FTC in a hybrid London setup.

Formación

  • Degree in Pharmacy, Life Sciences, or a related healthcare discipline.
  • Minimum 2 years' experience in Quality Assurance within the pharmaceutical, biotech, or healthcare industry.
  • Good understanding of Quality Management Systems, GDP, and relevant pharmaceutical regulations.
  • Experience managing deviations, CAPAs, change controls, and documentation systems.
  • Strong process improvement and continuous improvement mindset.
  • Experience writing SOPs, process documentation, and process mapping.
  • Excellent attention to detail and organisational skills.
  • Adaptable, proactive, and able to effectively manage multiple priorities.

Responsabilidades

  • Support the development, implementation, and maintenance of the Quality Management System (QMS).
  • Ensure compliance with Good Distribution Practice (GDP) requirements.
  • Manage quality processes including deviations, CAPAs, change controls, investigations, and risk assessments.
  • Review and approve quality-related documentation, SOPs, and controlled documents.
  • Maintain and administer electronic quality, training, documentation, reporting, and product database systems.
  • Support internal audits, inspections, and regulatory compliance activities.
  • Assist with product recall activities and provide GDP support when required.
  • Produce quality and training metrics and identify opportunities for process improvement.
  • Collaborate cross-functionally to promote a strong culture of quality and compliance.

Conocimientos

Quality Assurance
GDP compliance
QMS
CAPAs
Deviations
Change controls
Documentation
Risk assessment
Internal audits
Regulatory compliance

Educación

Pharmacy / Life Sciences degree

Descripción del empleo

Employment Type: FTC; Contract for 12-14months

Work Arrangement: Hybrid | Once a week in-office | London

Are you a Quality professional with experience in pharmaceutical quality systems and GDP compliance, looking to take on a broad and impactful role?

We're seeking a Quality Assurance Specialist to support and continuously improve the Quality Management System (QMS), ensuring compliance with regulatory requirements while driving quality, risk management, and continuous improvement initiatives across the business.

Key Responsibilities:
  • Support the development, implementation, and maintenance of the Quality Management System (QMS)
  • Ensure compliance with Good Distribution Practice (GDP) requirements
  • Manage quality processes including deviations, CAPAs, change controls, investigations, and risk assessments
  • Review and approve quality-related documentation, SOPs, and controlled documents
  • Maintain and administer electronic quality, training, documentation, reporting, and product database systems
  • Support internal audits, inspections, and regulatory compliance activities
  • Assist with product recall activities and provide GDP support when required
  • Produce quality and training metrics and identify opportunities for process improvement
  • Collaborate cross-functionally to promote a strong culture of quality and compliance
Qualifications:
  • Degree in Pharmacy, Life Sciences, or a related healthcare discipline
  • Minimum 2 years' experience in Quality Assurance within the pharmaceutical, biotech, or healthcare industry
  • Good understanding of Quality Management Systems, GDP, and relevant pharmaceutical regulations
  • Experience managing deviations, CAPAs, change controls, and documentation systems
  • Strong process improvement and continuous improvement mindset
  • Experience writing SOPs, process documentation, and process mapping
  • Excellent attention to detail and organisational skills
  • Adaptable, proactive, and able to effectively manage multiple priorities
Why Consider This Opportunity:
  • Broad QA role with exposure across quality systems, compliance, and continuous improvement
  • Opportunity to influence quality culture and business processes
  • Collaborative, cross-functional environment
  • Meaningful role supporting high standards of quality and patient care
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