Summary

I am hiring for a Senior QA Manager to join an innovative, growing biotechnology company with a developing clinical pipeline.

This is a senior QA position with broad responsibility across the organisation, supporting the progression of development programmes and providing quality leadership across the GxP landscape.

The role will work across GMP, GDP, and GCP, with particular responsibility for quality oversight of outsourced activities across CMC, manufacturing, testing, clinical supply, and clinical development.

You will work closely with internal scientific, clinical, and regulatory teams as well as external development, manufacturing, testing, and clinical service providers. The position offers the opportunity to take genuine ownership of quality activities, including vendor governance, quality agreements, audits, deviations, investigations, CAPAs, change controls, quality risk management, and inspection readiness.

A key part of the role will also be helping to develop and continuously improve a pragmatic, proportionate, and risk-based Quality Management System as the business continues to grow.

This is a hybrid role requiring 3 days per week onsite. This requirement is essential, so please do not apply if you are unable to commit to working onsite 3 days per week.

Responsibilities

• Provide QA leadership and oversight across GMP, GDP, and GCP activities.
• Develop, implement, and continuously improve risk-based QA policies, processes, procedures, and systems.
• Maintain and develop the Quality Management System in line with the organisation's evolving requirements.
• Provide QA oversight of outsourced development, manufacturing, testing, packaging, storage, and distribution activities.
• Establish appropriate quality governance, communication, and escalation arrangements with external partners.
• Lead the negotiation, approval, and maintenance of quality agreements.
• Monitor external partner performance, quality systems and controls, and manage associated risks and issues.
• Develop and manage a risk-based audit programme for GxP-critical suppliers.
• Plan and conduct vendor audits, issue reports, and oversee the implementation and closure of CAPAs.
• Provide QA oversight across CMC development, manufacturing, and testing activities.
• Review and approve relevant CMC, manufacturing, testing, and quality documentation.
• Provide QA oversight of clinical trial material supply, including manufacture, testing, release, packaging, labelling, storage, and distribution.
• Oversee quality events relating to clinical supply, including deviations, temperature excursions, complaints, and returns.
• Oversee deviations, investigations, CAPAs, and change controls across internal and outsourced activities.
• Lead or support root-cause investigations and quality risk assessments.
• Ensure appropriate corrective, preventive, and risk-mitigation actions are implemented and effectively closed.
• Provide QA oversight of clinical development activities in accordance with applicable GCP requirements, including ICH E6(R3).
• Support risk-based quality management and appropriate oversight of delegated clinical activities.
• Contribute to regulatory and inspection readiness activities, including preparation, responses, and follow-up.
• Review relevant regulatory documentation and submissions from a quality, compliance, and data integrity perspective.
• Act as a trusted QA partner to internal stakeholders across development and support functions.
• Provide clear, pragmatic, and proportionate quality advice across development activities.
• Contribute to the ongoing development of the organisation's quality strategy and culture.