QA Senior Manager in Thatcham

QA Senior Manager in Thatcham

Thatcham Full-Time 55200 - 55200 Β£ / year (est.) No working from home possible
Job Search Place Limited

At a Glance

  • Tasks: Lead global quality oversight and drive process improvements in a dynamic environment.
  • Company: Join a leading organisation focused on quality and compliance in clinical research.
  • Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
  • Other info: Be part of a proactive culture that values innovation and continuous improvement.
  • Why this job: Make a real impact by enhancing quality processes and ensuring compliance.
  • Qualifications: 8+ years in quality assurance or related fields; strong analytical and collaboration skills.

The predicted salary is between 55200 - 55200 Β£ per year.

Leads global process quality oversight activities by monitoring, trending, and evaluating escalations, quality events, audit/inspection outcomes, and other quality signals to identify potential systemic process failures. Partners with functional and operational teams to define, implement, and verify effective corrective and preventive actions through end-to-end management of global process CAPAs, supporting sustainable process improvement and inspection-ready quality governance.

Responsibilities

  • Monitor, review, and trend escalations, quality events, audit and inspection findings, process deviations, and other quality signals to identify recurring themes, emerging risks, and potential systemic process failures.
  • Lead assessment of whether identified trends represent isolated issues, functional gaps, or broader global process weaknesses requiring formal remediation.
  • Partner with process owners, operational leaders, RCQA stakeholders, and other cross-functional teams to define risk-based actions that address process gaps and prevent recurrence.
  • Own or support global process CAPAs from initiation through closure, including problem statement development, root cause evaluation, action planning, effectiveness measures, evidence review, and timely completion.
  • Ensure CAPA actions are appropriately scoped, achievable, inspection-defensible, and aligned with applicable controlled documents, regulatory expectations, and business process ownership.
  • Maintain visibility of global process CAPA status, risks, dependencies, and overdue or at risk actions, escalating appropriately to RCQA and functional leadership.
  • Develop and communicate quality insights, trend summaries, and process risk information to support management review, governance forums, and prioritisation of process improvement activities.
  • Facilitate cross-functional discussions to align on process gaps, ownership, action plans, implementation timelines, and objective closure evidence.
  • Use data analysis and quality intelligence to recommend targeted process improvements that increase process effectiveness, reduce repeat issues, and strengthen quality oversight across RCQA and operational processes.
  • Act as a process quality partner to operations and enabling functions, promoting a proactive culture of escalation, issue management, root cause thinking, and sustainable corrective action.
  • Support preparation for audits, inspections, sponsor inquiries, and internal governance discussions by ensuring process CAPA rationale, evidence, and effectiveness documentation are clear, complete, and defensible.
  • Contribute to global process governance forums by providing escalation trend analysis, systemic issue insights, CAPA progress updates, and recommendations for prioritisation.
  • Perform other duties as needed or assigned.

Qualifications

  • Bachelor's degree in Life Sciences, Quality, Regulatory Affairs, or related discipline preferred, or equivalent relevant experience.
  • Typically, 8 or more years of experience in regulated clinical research, GxP, quality assurance, regulatory compliance, process governance, or related environment.
  • Demonstrated experience with quality systems, CAPA management, root cause analysis, issue management, escalation handling, and/or process improvement in a regulated environment.
  • Strong understanding of applicable GxP regulations, quality standards, and expectations for inspection ready documentation.
  • Ability to analyse quality data, escalation trends, and recurring issue patterns to identify potential systemic process failures and recommend appropriate remediation.
  • Proven ability to collaborate, influence, and negotiate with cross functional stakeholders to achieve timely and sustainable process improvements.
  • Ability to distill complex quality information into clear conclusions, risk based recommendations, and management level communications.
  • Ability to lead or coordinate cross functional teams through CAPA development, implementation, effectiveness verification, and closure.
  • Experience preparing governance updates, quality summaries, or process risk communications for leadership forums preferred.

QA Senior Manager in Thatcham employer: Job Search Place Limited

Goldman Sachs is an exceptional employer, offering a dynamic work environment in the heart of London where innovation meets finance. With a strong emphasis on employee growth, comprehensive benefits including healthcare and competitive vacation policies, and a culture that fosters collaboration and creativity, this role as a VP Software Engineer provides a unique opportunity to be at the forefront of AI-driven technology in global markets.

Job Search Place Limited

Contact Details:

Job Search Place Limited Recruitment Team

We think you need these skills to ace QA Senior Manager in Thatcham

Process Quality Oversight
CAPA Management
Root Cause Analysis
Data Analysis
Quality Systems
Regulatory Compliance
GxP Regulations