Band 6 Biomedical Scientist Microbiology

Integrated Pathology Partnerships Limited

Information:

This job is now closed

Job summary

We are looking to speak with HCPC Registered Medical Microbiology/Infection Science Biomedical Scientists who have experience of providing a high-quality service and have a passion for mentoring and sharing your knowledge. The successful candidate would operate at our Hub laboratory in Taunton and you will be expected to participate in late shifts and on-call.

Monday - Sunday 08:30 - 17:00,

Late shifts Monday - Friday 12:30 - 20:00,

Out of Hours (On Call) - Monday - Friday 19:30 - 08:30

Out of Hours (On Call) - Saturday & Sunday 17:00 - 08:30

Main duties of the job

Our Infection Science Team operate across Microbiology, Virology and Molecular testing and we have a fantastic opportunity for an experienced Specialist Biomedical Scientist to join our team. This position is predominantly based in the Bacteriology department, working in a laboratory which takes a leading technological approach with a state-of-the-art automated analytical systems.

If you have the following qualifications and skills and feel that you could hit the ground running then wed love to hear from you:

  • Greater than 2 years post HCPC registration with experience of working in a busy clinical bacteriology department at post graduate level.
  • Experience working with Kiestra, MALDI-ToF, Phoenix and BacTec automated testing platforms
  • A strong clinical bacteriology background including knowledge of laboratory Quality Management systems.
  • A good understanding of clinical microbiology.

To operate at Band 6, you will also demonstrate experience to post graduate diploma level e.g.: Specialist portfolio.

About us

SYNLAB UK & Ireland work closely with clinicians, hospitals, occupational health providers and clinical researchers to provide a complete pathology offering.

We believe our staff are vital to the principle of making a positive difference to healthcare provision. 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.

Date posted

09 May 2024

Pay scheme

Other

Salary

£35,392 to £42,618 a year Joining bonus of up to £5,000

Contract

Permanent

Working pattern

Full-time

Reference number

E0308-24-0019

Job locations

I P P Facilities Ltd

Lisieux Way

Taunton

Somerset

TA1 2LB


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; Clinical Pathology Accreditation (CPA) Southwest Pathology Service policies and SOPs MHRA NHSCSP HTA HFEA 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.

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. Safety: To observe safety regulations and attend mandatory fire, manual handling and other courses 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 iPP policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies.

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; Clinical Pathology Accreditation (CPA) Southwest Pathology Service policies and SOPs MHRA NHSCSP HTA HFEA 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.

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. Safety: To observe safety regulations and attend mandatory fire, manual handling and other courses 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 iPP policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies.

Person Specification

Qualifications

Essential

  • HPC State Registration as a Biomedical Scientist with a Biomedical degree or equivalent and evidence of CPD.

Experience

Essential

  • Greater than 2 years post HCPC registration with experience of working in a busy clinical bacteriology department at post graduate level.
  • Experience working with Kiestra, MALDI-ToF, Phoenix and BacTec automated testing platforms
Person Specification

Qualifications

Essential

  • HPC State Registration as a Biomedical Scientist with a Biomedical degree or equivalent and evidence of CPD.

Experience

Essential

  • Greater than 2 years post HCPC registration with experience of working in a busy clinical bacteriology department at post graduate level.
  • Experience working with Kiestra, MALDI-ToF, Phoenix and BacTec automated testing platforms

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).

Employer details

Employer name

Integrated Pathology Partnerships Limited

Address

I P P Facilities Ltd

Lisieux Way

Taunton

Somerset

TA1 2LB


Employer's website

https://synlab.co.uk/ (Opens in a new tab)

Employer details

Employer name

Integrated Pathology Partnerships Limited

Address

I P P Facilities Ltd

Lisieux Way

Taunton

Somerset

TA1 2LB


Employer's website

https://synlab.co.uk/ (Opens in a new tab)

For questions about the job, contact:

Advanced Practitioner

Andrew Walker

andrew.walker@somersetft.nhs.uk

Date posted

09 May 2024

Pay scheme

Other

Salary

£35,392 to £42,618 a year Joining bonus of up to £5,000

Contract

Permanent

Working pattern

Full-time

Reference number

E0308-24-0019

Job locations

I P P Facilities Ltd

Lisieux Way

Taunton

Somerset

TA1 2LB


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