Specialist Biomedical Scientist- Blood Sciences

An exciting opportunity has arisen at The Christie Pathology Partnership (CPP) fora qualified and experienced Specialist Biomedical Scientist to join our Blood Sciences department on a 15-month fixed-term contract. The Christie is aworld-leading cancer treatment centre and a specialist site with no Accident& Emergency or Maternity services.

Thisis an exciting opportunity to contribute to a busy, high-quality diagnostic service at one of the UKs most respected specialist hospitals. The role operates within core laboratory hours only (Monday to Friday), with no requirement for shift or out-of-hours work. The role will involve working across all areas of Blood Sciences, though a background in Biochemistry is preferred.

Applications are welcomed from qualified Band 6 Biomedical Scientists, as well as experienced Band 5 Biomedical Scientists who are ready to develop into the role.

AtSYNLAB, we believe in nurturing a culture of well-being and ensuring our employees are supported both professionally and personally. That's why we'rethrilled 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.

• 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.

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

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

Webelieve our staff is vital 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 skillsand build their careers through learning and development opportunities,coaching and clear career pathways.

Please note that 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.

SYNLABUK & 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 all policies as required by regulatory directives, accreditation bodies and local management policies and practices.

Toprovide technical advice to clinical staff

Toperform and interpret routine and specialist Biomedical investigations and to participate daily in the scientific and technical activities of the laboratory section under the supervision of senior staff.

Togetherwith Senior staff help ensure compliance with all policies as required by regulatory directives, accreditation bodies and local management, including;

United Kingdom Accreditation Services (UKAS)

Christie Pathology Partnership policies and SOPs

MHRA

NHSCSP

HTA

HFEA

Anyother body in area of responsibility

Utilise the laboratory LIMS, Q-Pulse quality monitoring system and other application software according to authorised protocols including assisting in computer dataentry in all areas of the laboratory, document review, non conformance reviewand quality assurance processes.

Communicate efficiently, courteously and with clarity at all times, whether face to face,telephone or electronic methods referring enquiries to senior staff where appropriate. Matters being communicated may include complex information and/or results.

Attendand participate positively in laboratory and other meetings as directed by Laboratory senior staff

As directed by senior laboratory staff, plan and prioritise work allocations,training plans, audits of both yourself and junior staff, responding appropriately to the needs of routine and urgent activities.

Encourage active participation in continuous professional development and support the introduction of new technologies and / or systems by being a change advocate.

Reportall incidents and adverse events to senior…