Job summary
Biomedical Scientist Permanent
Band 5 - £29,970 £36,483
(WTE), Full-time (37.5 hours per week)
Additional Wellbeing
Allowance - £1,500 per annum (pro-rata)
An
exciting opportunity has arisen at The Christie Pathology Partnership (CPP) for
a Biomedical Scientist to join our Histology department.
About us
The Christie Pathology
Partnership was formed in 2014 and is a joint venture 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, the largest single site cancer
centre in Europe, treating more than 60,000 patients a year and the first UK
centre to be accredited as a comprehensive cancer centre.
SYNLAB is the European leader
in delivery of high-quality pathology testing and imaging services. SYNLAB
operates in 35 countries across four continents, employing more than 20,000
members of staff and conducting approximately 500 million tests per annum.
Main duties of the job
To be able to rotate through all areas of the
Laboratories as required (Dependent on qualifications, experience and
training), to perform all designated duties in accordance with local working
practices, to maintain high Professional standards and conform to Health and
Safety regulations. To perform
Biomedical investigations autonomously, within operating procedures and
protocols, to provide within agreed quality standards of service delivery and
turnaround times under the supervision of senior grade BMS grade staff. To
continue with personal development through academic or practical experience. To
provide professional leadership and supervise Trainee BMS, Associate
Practitioners and Medical Laboratory Assistants. To maintain the standards of
conduct required by the Health Professions Council to practice as a registered
Biomedical Scientist.
The
successful candidate will have:
A BSc
(Hons) Biomedical degree or equivalent
HCPC State
Registration as a Biomedical Scientist
SYNLAB
is a committed equal opportunities employer and we are open to flexible working.
Applicants
must currently have permission to work in the UK.
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 are 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
Be able to rotate through all areas of the laboratory required (dependent on qualifications, experience and training) performing all
designated duties in accordance with local working practices whilst maintaining high Professional standards and conforming to Health and
Safety regulations.
Maintain the standards of conduct required by the HPC to practice as a registered Biomedical Scientist.
Provide specialist technical advice to clinicians as to the appropriateness of tests and timescales.
Perform routine and specialist biomedical investigations, and participate daily in the scientific and technical activities of the laboratory
section, which may include specimen reception functions, under the supervision of Senior Biomedical Scientists.
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. Propose
changes to standard operating procedures as required in order to develop and streamline the service or to reflect other changes.
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.
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 managers
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.
Provide supervision, training and professional leadership to junior staff which includes monitoring their performance against laboratory
standards and their training plans.
Encourage active participation in continuous professional development and support the introduction of new technologies and / or systems
by being a change advocate, and active mentor and a tutor to junior staff.
Use consumables and equipment within your allocated section responsibility and be responsible for stock control audits and recording
through approved channels as required.
Report all incidents and adverse events to senior staff and enter the information in the CAPA module of Q-pulse in a timely manner as
directed by senior staff.
Demonstrate on going competency against training plans.
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.
Safety:
To observe safety regulations and attend mandatory fire, manual handling and other course as required.
To assist in the investigations of any incidents.
Participate in risk assessment monitoring
To ensure that the equipment within area of work is maintained and operated as per SOPs
To comply with CPP policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies
Job description
Job responsibilities
Be able to rotate through all areas of the laboratory required (dependent on qualifications, experience and training) performing all
designated duties in accordance with local working practices whilst maintaining high Professional standards and conforming to Health and
Safety regulations.
Maintain the standards of conduct required by the HPC to practice as a registered Biomedical Scientist.
Provide specialist technical advice to clinicians as to the appropriateness of tests and timescales.
Perform routine and specialist biomedical investigations, and participate daily in the scientific and technical activities of the laboratory
section, which may include specimen reception functions, under the supervision of Senior Biomedical Scientists.
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. Propose
changes to standard operating procedures as required in order to develop and streamline the service or to reflect other changes.
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.
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 managers
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.
Provide supervision, training and professional leadership to junior staff which includes monitoring their performance against laboratory
standards and their training plans.
Encourage active participation in continuous professional development and support the introduction of new technologies and / or systems
by being a change advocate, and active mentor and a tutor to junior staff.
Use consumables and equipment within your allocated section responsibility and be responsible for stock control audits and recording
through approved channels as required.
Report all incidents and adverse events to senior staff and enter the information in the CAPA module of Q-pulse in a timely manner as
directed by senior staff.
Demonstrate on going competency against training plans.
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.
Safety:
To observe safety regulations and attend mandatory fire, manual handling and other course as required.
To assist in the investigations of any incidents.
Participate in risk assessment monitoring
To ensure that the equipment within area of work is maintained and operated as per SOPs
To comply with CPP policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies
Person Specification
Qualifications
Essential
- BSc (Hons) Biomedical degree or equivalent
- HCPC State Registration as a Biomedical Scientist
Person Specification
Qualifications
Essential
- BSc (Hons) Biomedical degree or equivalent
- HCPC State Registration as a Biomedical Scientist
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).