PE Global is currently recruiting for a Senior Quality Associate on behalf of a leading global pharmaceutical organisation.
Location: Bracknell
Contract duration: 12 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 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.
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