PE Global is currently recruiting for a Senior Quality Associate on behalf of a leading global pharmaceutical organisation.
Contract duration: Hourly rate: £22.42-£29.89 per hour
You will provide quality oversight across business processes, support audits and inspections, manage deviations and CAPAs, and collaborate cross-functionally to strengthen quality culture and operational excellence.
Quality Systems & Compliance
Support the implementation and management of quality systems and regional quality plans
Review and contribute to quality procedures, templates, and controlled documentation
Partner with business stakeholders to interpret regulatory and quality requirements
Quality Oversight
Provide quality guidance and consultation across affiliate business functions
Support risk assessments, quality planning, and continuous improvement initiatives
Monitor quality actions arising from audits, inspections, and deviations
Audits & Inspection Readiness
Assist with inspection readiness and audit response management
Maintain accurate and inspection-ready documentation and training records
Act as a trusted quality partner for assigned business areas
Build strong working relationships with internal stakeholders and quality networks
Contribute to key quality and business projects as required
Promote a risk-based and compliant approach across operations
Bachelor’s or Master’s degree in a scientific, healthcare, or related discipline
Minimum 3 years’ experience in Quality, Regulatory, Clinical Development, Pharmacovigilance, or related GxP environments
Strong understanding of quality systems within regulated industries (GMP, GCP, GVP)
Contract duration: Hourly rate: £22.42-£29.89 per hour
You will provide quality oversight across business processes, support audits and inspections, manage deviations and CAPAs, and collaborate cross-functionally to strengthen quality culture and operational excellence.
Quality Systems & Compliance
Support the implementation and management of quality systems and regional quality plans
Review and contribute to quality procedures, templates, and controlled documentation
Partner with business stakeholders to interpret regulatory and quality requirements
Quality Oversight
Provide quality guidance and consultation across affiliate business functions
Support risk assessments, quality planning, and continuous improvement initiatives
Monitor quality actions arising from audits, inspections, and deviations
Audits & Inspection Readiness
Assist with inspection readiness and audit response management
Maintain accurate and inspection-ready documentation and training records
Act as a trusted quality partner for assigned business areas
Build strong working relationships with internal stakeholders and quality networks
Contribute to key quality and business projects as required
Promote a risk-based and compliant approach across operations
Bachelor’s or Master’s degree in a scientific, healthcare, or related discipline
Minimum 3 years’ experience in Quality, Regulatory, Clinical Development, Pharmacovigilance, or related GxP environments
Strong understanding of quality systems within regulated industries (GMP, GCP, GVP)
