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