HCPC Sign Out Manager

Job Description

This is temporary contract until March 2022, working on a 4 days on and off shift pattern- 4 weeks of 8am-8pm and 4 weeks of 8pm-8am. You must be HCPC registered to apply.Job Purpose:

1. The analysis of Real Time PCR data generated by the clinical laboratory team to provide results of COVID 19 diagnosis.
2. To provide assurance to the Laboratory Senior Management team, through data analysis of the credibility of test results produced within the laboratory.
3. To assist the Laboratory Shift Manager & Lead Scientist in the management of the laboratory.

Managerial

1. Leads and manages a team of Analysts ensuring the quality of results
2. Acts as a clinical expert leading reviews of queries and anomalies
3. Review test results, maintains legible work records and enters findings into the laboratory information system (LIMS).
4. Participates, as requested, in training of new employees
5. Achieve, demonstrate, maintain and promotes scientific & technical excellence, and by example ensure high professional standards amongst the scientific, technical and support staff within the laboratory.
6. To ensure that all staff meet the necessary standards of speed, quality and accuracy, appropriate to the level of experience and training.
7. To be support the induction, training & competencies of staff within the section. This includes ensuring contemporaneous completion of all induction, training & competency records.
8. Support and help to develop the training of the laboratory staff at all levels.
9. Work with and supervise the work of staff in conjunction with other senior members of staff.
10. Working with the Laboratory Shift Manager, Lead Scientist, develop, coordinate and maintain the laboratorys programme of continuous service review in accordance with internal and external quality systems and within the framework of continuous quality improvement.
11. To work with the quality manager to ensure all necessary quality standards are met, including UKAS ISO15189.
12. To be responsible for the establishment, and participate in the auditing, of all working procedures and protocols within your area of responsibility.
13. To be responsible for the promotion, identification and implementation of efficiency measures within the section. Work with senior staff in the other sections to ensure that any efficiency measures identified within the section are implemented.
14. To be responsible for the production of all standing operational procedures, protocols and policies within the section, and ensure that they are maintained, reviewed and updated when necessary.
15. To be responsible for implementing any procedural changes required by the Laboratory Shift Manager and disseminate information relating to them.
16. To be responsible for the accurate maintenance of all records pertaining to the activities of the areas of responsibility.
17. Together with the section leads, take a shared responsibility for the fabric of the laboratory.
18. To be responsible for the identification, recording, assessment and mitigation of risks within the section, and escalate where appropriate to shift manager
19. Dress and act in a professional manner and set an appropriately high example of conduct.
20. Prepare and provide statistical and other information as required.
21. Provide workload statistics.
22. To be responsible for the participation in and adherence to the procedures for both internal and external quality control (including national External Quality Assurance Schemes, NEQAS), thereby providing quality assurance in test results produced.

Essential Knowledge and experience

• Scientific knowledge in molecular biology of infectious diseases/genetic diorders
• An understanding of the meaning of results to enable authorisation and appropriate action in dealing with abnormal or unusual results
• A working knowledge and practical application of the departments IT systems
• Experience in a laboratory preferably in molecular or microbiology.
• Team leadership skills
• Computer literacy, with a working knowledge of Microsoft Word & Excel
• Experience of UKAS ISO 15189 Accreditation, audit and management
• Educated to BSc (Hons)
• Required to work in an area of biological risk, frequently exposed to biological and chemical hazards and with the requirement to remove unpleasant bodily fluids, eg. urine, faeces, sputum etc. from their containers for analysis.
• in Biomedical Sciences or equivalent qualification acceptable to the Institute of Biomedical Sciences and the Health Professions Council for registration