Specialist Biomedical Scientist - Blood Sciences

Specialist Biomedical Scientist - Blood Sciences

The Clinical Pathology Partnership (CPP) Blood Sciences Department, based on-site at The Christie Hospital, is seeking an experienced and motivated Specialist Biomedical Scientist to join our team. The Christie is a world-leading cancer treatment centre and a specialist site with no Accident & Emergency or Maternity services.

The Christie Pathology Partnership was formed in 2014 and is a joint enterprise between The Christie NHS Foundation Trust and SYNLAB, the largest provider of laboratory pathology and diagnostic services in Europe. We provide Pathology services for The Christie, which is the largest single cancer centre site in Europe and the first UK centre to be accredited as a comprehensive cancer centre.

The Christie treat more than 60,000 patients a year.

This is an exciting opportunity to contribute to a busy, high-quality diagnostic service at one of the UKs most respected specialist hospitals. This is a full-time permanent role and you will be expected to participate 24/7 rota.

At SYNLAB, we believe in nurturing a culture of well-being and ensuring our employees are supported both professionally and personally. That's why we're thrilled to offer an exhilarating rewards package, including our incredible Wellbeing Allowance worth up to £1500 per annum for our esteemed team members working in Band 2 - 8 roles.

Our Haematology Biochemistry laboratory processes approximately 720,000 samples per year and is equipped with Siemens Atellica and Advia analysers, Coagulation ACL Tops and manual assays/techniques supporting both a Core Biochemistry & Haematology Laboratory. Together, these laboratories deliver a comprehensive service including tumour marker monitoring for patients undergoing cancer treatment.

• Perform and interpret complex analytical investigations within Blood Sciences.
• Provide specialist advice on troubleshooting analyser and assay issues.
• Undertake validation and verification of new methods and equipment.
• Participate in EQA (External Quality Assessment) interpretation and reporting.
• Contribute to training and supervision of less experienced staff.
• Engage actively in quality management, including internal audits and document review.
• Operate and maintain competence with the Laboratory Information Management System (LIMS) and associated middleware applications.

SYNLAB UK & Ireland work closely with clinicians, hospitals, occupational health providers and clinical researchers to provide a complete pathology offering.

We operate in increasingly diverse environments which is reflected in our workforce, clients,customers, suppliers, communities and partners. We believe an inclusive workplaceculture is the best way to source, attract and retain diverse and talented people, and create a sustainable, high-performing workforce.

We believe our staff isvital to the principle of making a positive difference to healthcare,therefore, we promote a culture of continuous personal development where scientists and staff have the support and resources to acquire new skills andbuild their careers through learning and development opportunities, coaching and clear career pathways.

We promote an open and collaborative culture where leaders act as role models and facilitate a two-way communication, engage with staff and stakeholders transparently and actively encourage feedback and suggestions.

We reserve the right to close any adverts once we have received asufficient number of applications. If you decide to apply for this post but donot hear back from us within two weeks of your application, please assume thatyou have not been short-listed on this occasion.

SYNLAB UK& Ireland is a committed equal opportunities employer and does not unlawfully discriminate on the basis of any status or condition protected by applicable UK employment law.

Participate in and assist with clinical trials, the development of new tests and research& validation of equipment ensuring at all times compliance with allpolicies as required by regulatory directives, accreditation bodies and local management policies and practices.

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