Job summary
We are currently recruiting for Specialist Biomedical Scientists to join our fast paced and dynamic Microbiology team. This role is part of a team which provides an efficient and effective Microbiology service to two general hospitals (Southend University/Basildon and Thurrock University Hospital Trusts) and local GP community.
We're the first lab in the UK to be able to offer some Specialist BMS staff the opportunity to read bacterial cultures from home, utilising BD Kiestra Synapsys technology.
Main duties of the job
The postholder will be expected to be able to rotate through all areas of Microbiology as required, and to perform all designated duties in accordance with local working practices. You will need to perform and interpret routine and specialist biomedical investigations autonomously and to provide patients results within agreed quality standards of service delivery and turnaround times under the supervision of senior staff. You will need to provide professional leadership to Trainee BMS, Associate Practitioner, Laboratory technicians and MLAs in Bacteriology, Molecular biology, and Serology and provide technical advice to clinicians as to the appropriateness of tests and timescales.
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.
We reserve the right
to close any adverts once we have received a sufficient number of applications.
If you decide to apply for this post but do not hear back from us within two
weeks of your application, please assume that you 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.
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: iPP 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: iPP 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
Qualifications
Essential
- HCPC State Registration as a Biomedical Scientist with a Biomedical Science degree or equivalent and
- evidence of CPD
- Experience to post graduate diploma level e.g.: Specialist portfolio, BBTS
Experience
Essential
- At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training.
Person Specification
Qualifications
Essential
- HCPC State Registration as a Biomedical Scientist with a Biomedical Science degree or equivalent and
- evidence of CPD
- Experience to post graduate diploma level e.g.: Specialist portfolio, BBTS
Experience
Essential
- At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training.
Additional information
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
