Job summary
We
are seeking an enthusiastic and motivated Specialist Biomedical Scientist in Clinical
Biochemistry to join our Blood Sciences team.
Pathology
First operates over three sites using a hub and spoke model. Our hub site
offers a high throughput service for our non-urgent community work, and
specialist testing for specific proteins. Our two hospital laboratories at
Southend and Basildon provide urgent testing for acute admissions and
inpatients. This role will involve rotating across sites. Our laboratories
receive approximately 1.2 million clinical biochemistry requests per year, on
which we do approximately 12 million tests. The main analyser platforms are
Beckman Coulter, fully tracked at the hub laboratory, backed up with Roche. The
hospital repertoire includes CO2, lactate, osmolality, ammonia, bile
acids, troponin T, BNP, xanthochromia, haematinics, therapeutic drugs, thyroid
hormones, procalcitonin, prolactin, BHCG and cortisol. The hub laboratory
repertoire is more extensive with three different immunoassay platforms. The
main IT platform for all sites is Clinisys WinPath Enterprise.
Main duties of the job
You
will need to be flexible to fit in with our multi-site, around the clock shift
pattern (unsocial shifts attract additional payments). The environment is fast-paced
offering a one-hour turnaround time to acute users, two hours for inpatients
and four hours for community requests. You will require specialised knowledge
and experience of laboratory techniques, analyser platforms and associated
equipment. As a specialist you will independently validate all clinical
biochemistry investigations. You will have a role in the training of less
experienced employees, and you will be involved in quality management including
auditing and document review. You will need to be conversant with the main
laboratory information management system and middle-ware applications. We will
consider sponsoring suitable employees on a relevant MSc course.
About us
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 workplace culture is the best way to source, attract and retain
diverse and talented people, and create a sustainable, high-performing
workforce.
We
believe 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 skills
and build their careers through learning and development opportunities,
coaching and clear career pathways.
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.
Job description
Job responsibilities
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.
To provide technical advice to clinical staff.
To perform 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.
Together with Senior staff help ensure compliance with all policies as required by regulatory directives,
accreditation bodies and local management, including. SYNLAB policies, MHRA, NHSCSP, HTA, HFEA, United Kingdom Accreditation Service (UKAS) and Any other 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 data entry in all areas of the laboratory, document review,
non-conformance review and 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.
Attend and 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.
Report all incidents and adverse events to senior staff.
Demonstrate on going competency against training plans and participate positively in CPD (continuous
professional development) activities.
Job description
Job responsibilities
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.
To provide technical advice to clinical staff.
To perform 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.
Together with Senior staff help ensure compliance with all policies as required by regulatory directives,
accreditation bodies and local management, including. SYNLAB policies, MHRA, NHSCSP, HTA, HFEA, United Kingdom Accreditation Service (UKAS) and Any other 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 data entry in all areas of the laboratory, document review,
non-conformance review and 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.
Attend and 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.
Report all incidents and adverse events to senior staff.
Demonstrate on going competency against training plans and participate positively in CPD (continuous
professional development) activities.
Person Specification
Experience
Essential
- At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training
Qualifications
Essential
- HCPC registered as a Biomedical Scientist
- IBMS Specialist Diploma in Clinical Biochemistry, or equivalent specialist qualifications
Person Specification
Experience
Essential
- At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training
Qualifications
Essential
- HCPC registered as a Biomedical Scientist
- IBMS Specialist Diploma in Clinical Biochemistry, or equivalent specialist qualifications
Additional information
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
