Job summary
An exciting opportunity has arisen to undertake the role of Lead Quality Specialist (may be equivalent to Head of Quality in other NHS organisations) in NHS Blood and Transplant (NHSBT). We are looking for an experienced senior leader who is enthusiastic and passionately strives for improvement and excellence.
NHSBT has a vision of a world where every patient receives the donation they need. It will achieve this by maintaining high quality and caring standards of products and services, whilst utilising its expertise.
The post holder will be responsible for developing, implementing, and monitoring an effective, safety focussed and compliant quality management system (QMS). The successful candidate will be assigned to a Directorate or function (, Technical Assurance, Blood Supply, Clinical Services, Plasma, Quality Management Systems etc), whilst providing support for other areas of the organisation as appropriate.
The post holder will be a key member of the Quality senior management team (Q-SMT), supporting the Quality Directorate in achieving its strategic objectives, whilst also ensuring our core business as usual activities are maintained and improved. The successful candidate will be required to horizon scan, provide guidance and support based on best practices, develop a culture of collaboration, innovation, informed questioning and challenging, trend analysis triangulation, risk awareness, proportionate response and proactively engage with quality improvement.
Main duties of the job
The post holder will be required to :
- Providing visible senior leadership and oversight of the quality and safety agenda in collaboration with other stakeholders, , Risk, Business Continuity, Clinical Governance, ensuring attainment of real improvements for patient and donor safety.
- Leading portfolio(s) or key programmes of work arranged within a Directorate or across the organisation, supporting quality management, improvement, and safety system approaches as designated.
- Providing line management of staff, teams, or functions within portfolio or across a matrix.
- Provide safety compliance and regulatory expertise to operational areas for business-as-usual activities, and where we are developing new services and products.
- Taking ownership and accountability for the status of the QMS aligned with the supported Directorate, and ensure it is maintained and developed.
- Develop, implement, monitor, and improve the necessary quality expertise and systems required primarily by the supported Directorate(s) to deliver an efficient and effective, nationally consistent, and accredited QMS and GMP system. The post holder will ensure a validated QMS is always maintained to provide safe and efficacious products and services for patients and donors.
- Support the Assistant Director of Quality and Regulatory Compliance in the development and delivery of a Quality Strategy which support NHSBT and its delivery and safety focus.
About us
It takes all types of people to deliver the kind of service that saves and improves lives. At NHS Blood and Transplant, you will join a team of more than 6,000 people who are making a genuine difference to communities, families, friends, relatives and more across the UK. We play a unique and special role in the NHS by helping people do something extraordinary- donate blood, blood products, organs, tissues, or stem cells to save someone in need. Our three core values are what set us apart. They guide and inspire everything we do. By being caring, expertly meeting the needs of our patients and our people, and accepting nothing less than the best quality, we can do extraordinary work and help our people to do something extraordinary in their career, too. Three small words, one big difference - Caring, Expert and Quality. Together we'll save and improve more lives than ever.
Job description
Job responsibilities
Please view the attached recruitment profile which is a summary of the detailed Job Description and Person Specification for the full personal attributes we require for the role. You will need to demonstrate these throughout the recruitment process.
Person Specification
Qualifications
Essential
Masters in a bio-medical or pharmaceutical subject with examination via professional body. OR extensive relevant experience to masters level.Demonstrates commitment to own continued professional development (CPD).Experience
Essential
Significant experience of leading a quality and improvement team.Experience of co-production with stakeholders-service users.Substantial project management, performance management, strategic planning, and risk identification and management experience.Experience of leading and implementing significant change projects- programmes.Proven record of developing and maintaining an effective QMS and information resources to drive innovation within a service.Experience of working with minimal supervision, working alone and within a team -amongst teams.Substantial experience as a senior quality professional in a regulated (Good Pharmaceutical Manufacturing Practice, NHSBT or equivalent) environment.Working knowledge of relevant legislation and components of quality, safety, risk, governance and assurance functions, for example the EU Blood Safety Directives and other mandated accreditation schemes.Experience of coaching colleagues to take responsibility for their own development and work through self and group accountability, varied assignments, and on-going feedback, using bank of experience to provide examples to those they coach.Working knowledge of Freedom of Information, EU General Data Protection Regulation (UK Data Protection Act), Good Automated Manufacturing Practice and related legislation including recognised international quality standards.Specialist knowledge of the physiology and pharmacology of blood and tissues and their use in transfusion and transplantation.