Senior Quality Associate

PE Global is currently recruiting for a Senior Quality Associate on behalf of a leading global pharmaceutical organisation.

Be one of the first applicants, read the complete overview of the role below, then send your application for consideration.

Location: Bracknell

Contract duration: 6 months

Hourly rate: £22.42-£29.89 per hour

The Role

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.

Key Responsibilities

Quality Systems & Compliance

• Support the implementation and management of quality systems and regional quality plans
• Manage deviations, change controls, CAPAs, and management notifications
• Conduct root cause investigations and ensure effective corrective and preventative actions
• Review and contribute to quality procedures, templates, and controlled documentation
• Partner with business stakeholders to interpret regulatory and quality requirements
• Monitor compliance trends and proactively identify areas for improvement

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
• Drive standardisation and share best practices across regional and global teams

Audits & Inspection Readiness

• Support and coordinate internal and external audit activities
• Assist with inspection readiness and audit response management
• Ensure timely closure of audit findings and CAPA commitments
• Maintain accurate and inspection-ready documentation and training records

Cross-Functional Partnership

• 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

Candidate Requirements

• 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 xwzovoh environments
• Strong understanding of quality systems within regulated industries (GMP, GCP, GVP)
• Experience managing deviations, CAPAs, change controls, and audit activities
• Excellent analytical, problem-solving, and organisational skills
• Strong written and verbal communication skills with the ability to influence stakeholders
• Ability to manage multiple priorities in a fast-paced environment
• Experience working within global or matrix organisations is advantageous

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

Interested candidates should submit an updated CV.

Please click the link below to apply.