Job Title

Quality Oversight and Compliance Manager UK 6-Month Contract | 26.2132.00 per hour (Umbrella) I Hours: 37 per weekLocation: Onsite Sandwich or Tadworth I Remote option (with occasional office visits)Were partnering with a leading global pharmaceutical company to recruit a Quality Oversight and Compliance Manager. This is a key role focused on improving regulatory quality, process compliance, and inspection readiness across a global regulatory landscape.Youll work cross-functionally with Regulatory Strategy, Submissions, CMC, and Information Management teams to support continuous improvement in regulatory processes and data governance. This is a great opportunity to bring your regulatory knowledge, analytical mindset, and project leadership skills into a role with meaningful global impact.What You'll Be Doing:Drive Process Improvement: Identify opportunities for improvement in global regulatory and submission processes, leveraging data and metric analysis.Lead Compliance Activities: Address procedural and compliance gaps, establish remediation plans with stakeholders, and track progress.Audit and Inspection Readiness: Support business teams in preparing for audits and inspections. Provide follow-up on findings, coordinate corrective actions, and track progress.Quality Events and CAPA Management: Lead or contribute to investigations of quality events, ensuring timely implementation of CAPA plans.Data & Metrics Analysis: Generate reports and presentations for senior leadership, highlighting trends and performance in compliance activities.Stakeholder Engagement: Partner with cross-functional global teams to align on quality strategy and ensure best practices are shared and embedded across the organisation.Support Change and New Initiatives: Participate in change initiatives, new technology implementations, and training efforts aimed at improving regulatory quality and consistency.What Youll Bring:Solid understanding of global regulatory strategy, regulatory affairs, and submission managementDemonstrated success managing quality investigations, CAPAs, and compliance improvementsStrong data analysis and reporting skillsable to turn data into actionable insightsAbility to influence and collaborate effectively across global matrix teamsProficient in managing change, implementing process improvements, and working in regulated environmentsQualifications:BSc, MSc, or PhD in life sciences or a related fieldExperience in a global pharmaceutical or regulatory settingStrong written and verbal communication skillsAdvanced organisational and analytical capabilitiesIf youre a proactive, detail-oriented professional ready to support global regulatory quality excellence, wed love to hear from you!