Senior Biomedical Scientist

1 week ago


Basildon, Essex, United Kingdom iPP Analytics Limited Full time

Job Summary

We are seeking an experienced Biomedical Scientist to join our dynamic Cellular Pathology Department, providing an efficient and effective Histology and Diagnostic (Non Gynae) Cytology service to two general hospitals and local GP surgeries/community clinics.

As a core member of the team, your role will make a positive difference to our healthcare service. You will receive regular training and coaching to develop your skills in your working role. This is a great step up for a Biomedical Scientist into a Specialist role.

Main Duties of the Job

  • Undertake routine and specialised laboratory techniques in the processing of Diagnostic Cytology (Non Gynae).
  • Support laboratory staff with any queries for the non-Gynae sample and troubleshoot the problem when needed regarding acceptance and processing of the sample.
  • Be always ready and willing to cover any step in Non Gynae sample processing, staining, pre-screening and sending cases to the pathologists.
  • Work within health and safety guidelines.
  • Provide patients with the highest level of diagnosis process within agreed quality standards of service delivery and turnaround times under the supervision of senior grade BMS staff.
  • Be part of the Laboratory Non gynae pre-screen team and help oversee the service, in the absence of the Cytology Advanced Practitioner.

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.

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.

Provide technical advice to clinical staff.

Perform and interpret routine and Specialist Biomedical investigations and 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 ongoing 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 ongoing 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

  • IBMS Accredited BSc in Biomedical Science or equivalent
  • HCPC registered Biomedical Scientist
  • IBMS Specialist Diploma in Cellular Pathology

Experience

Essential

  • Knowledge and experience of Histology/Diagnostic (Non Gynae) Cytology processing, techniques, pre-screening and practices at post honours degree level
  • Show the understanding and importance of Quality Control and Quality Assurance procedures in the department (staining IQC).
  • Contribute towards overall upkeep of Diagnostic Cytology section by supporting staff, completing tasks in timely manner, maintaining Turn Around Times and devoting time productively in other tasks of Diagnostic Cytology/Histology department.
  • Ability to work across 3 different sites in a 24-7 work environment if/and when required.
  • Able to demonstrate a good knowledge and experience of industry standard laboratory information management systems and computer applications including Word, Excel, Power Point, Access and Statistical Packages.

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