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.