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. Applicants must currently have permission to work in the UK.
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.
As an important member of our team, you will be fundamental in making a positive difference to our healthcare service. You will receive regular training and coaching to develop your skills and to support you in your working life. We seek candidates who are passionate with good interpersonal skills and the drive to develop their career within our supportive environment.
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 - 6 roles. Additionally, for band 5 & 6 roles, where night shift is part of the role requirements, you will receive enhanced night shift payment.
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.
- Role specific - Automation Laboratory - Kiestra TLA, MRSA and Urogenital Sections
- Role specific - Automation Laboratory Automated ID, AST, reading room and wound swab sections
- Role specific - Manual Bacteriology CL3, Mycology and Waste Management
- Role specific - Manual Bacteriology Blood culture, Sterile body fluid, Faeces, Environmental sections
- Role specific - NAATs and urinalysis
- Role specific Serology
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 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 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)
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.
Other:
Be
an ambassador for Diversity and Inclusion.
Communicate
and role model the values and behaviours of SYNLAB.
Communicate
efficiently, courteously and with clarity at all times, whether face to face,
telephone or electronic methods referring enquiries to senior staff where
appropriate.
Undertake
any other reasonable duty, when requested to do so by an appropriate manager.
Demonstrate
on going competency against training plans and participate positively in CPD
(continuous professional development) activities.
Complete
all statutory, mandatory and essential training within timeframes specified.
Safety:
Observe
safety regulations and attend mandatory fire, manual handling and other courses
as required.
Report
all incidents and adverse events to managers and assist in the investigations
of any incidents.
Participate
in risk assessment monitoring.
Ensure
that the equipment within area of work is maintained and operated as per SOPs.
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)
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.
Other:
Be
an ambassador for Diversity and Inclusion.
Communicate
and role model the values and behaviours of SYNLAB.
Communicate
efficiently, courteously and with clarity at all times, whether face to face,
telephone or electronic methods referring enquiries to senior staff where
appropriate.
Undertake
any other reasonable duty, when requested to do so by an appropriate manager.
Demonstrate
on going competency against training plans and participate positively in CPD
(continuous professional development) activities.
Complete
all statutory, mandatory and essential training within timeframes specified.
Safety:
Observe
safety regulations and attend mandatory fire, manual handling and other courses
as required.
Report
all incidents and adverse events to managers and assist in the investigations
of any incidents.
Participate
in risk assessment monitoring.
Ensure
that the equipment within area of work is maintained and operated as per SOPs.
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
- At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training.
Skills
Essential
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
- At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training.
Skills
Essential
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
