Job summary
We are expanding and are looking for an experienced Specialist Biomedical Scientist (BMS) who is ready to advance their career aspirations in a supportive and collaborative environment. At SYNLAB/Pathology First, we believe in building a strong, collaborative team where individuals are encouraged to grow with us, not just work for us.
We offer ongoing training and mentorship to help you further develop your existing skill set and advance within our organisation (we happen to be the largest clinical diagnostics company in Europe!). We are proud to be the first lab in the UK to offer some of our BMS staff the opportunity to read bacterial cultures from home, using cutting-edge BD Kiestra Synapsys technology. This role is based at our Hub site in Basildon.
Our Commitment to You:
We understand that a great work environment is built on support and care. Our rewards package is designed to support your personal and professional well-being, including our incredible Wellbeing Allowance of up to £1500 per annum for our team members in Band 2-6 roles, as well as enhanced night shift payments for Band 5 & 6 roles.
There is also a £5,000 Joining Bonus for qualified Band 6 BMSs.
Main duties of the job
You
will be a fundamental part of our close-knit Microbiology team, providing an
efficient and effective service to two general hospitals and the local GP
community. In this role, you will:
Perform and interpret routine and specialist biomedical investigations.
Provide professional leadership to Trainee BMS, Associate Practitioners,
Laboratory technicians, and MLAs.
Offer technical advice to clinicians on the appropriateness of tests and
timescales.
Rotate through all areas of Microbiology, including:
Automation Laboratory - Kiestra TLA, MRSA, and Urogenital Sections
Manual Bacteriology CL3, Mycology, and Waste Management
NAATs and urinalysis
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, 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
Experience
Essential
- Working knowledge of Microbiological manual and automated techniques and practices.
- Working knowledge of serology and Molecular biology techniques and platforms.
Qualifications
Essential
- HCPC registered, have at least 2 years post registration experience and have a Specialist portfolio or equivalent in Microbiology. We will consider applications from people nearing the completion of their specialist portfolio.
- Biomedical Science degree or equivalent and evidence of CPD
Person Specification
Experience
Essential
- Working knowledge of Microbiological manual and automated techniques and practices.
- Working knowledge of serology and Molecular biology techniques and platforms.
Qualifications
Essential
- HCPC registered, have at least 2 years post registration experience and have a Specialist portfolio or equivalent in Microbiology. We will consider applications from people nearing the completion of their specialist portfolio.
- Biomedical Science degree or equivalent and evidence of CPD
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.
