Quality Officer

at  Synnovis

London SE1 8NZ, , United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Dec, 2024GBP 57802 Annual21 Sep, 2024N/AGood communication skillsNoNo
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Description:

We’re looking for a highly motivated Quality Officer to join the Quality Team at Synnovis Analytics. The role is based on the Guy’s and St Thomas’ Hospital sites and at the Synnovis Blackfriars Hub laboratories, in the Haematology and Blood Transfusion services.
Synnovis Analytics is fortunate to have a strong Quality Team, and the successful candidate will be an integral part of this team. We work together in a supportive framework to move forward quality management and governance processes within Synnovis in conjunction with our operational and clinical colleagues, within Synnovis and our partner NHS Trusts.
You will have HCPC State registration as a Biomedical Scientist or Clinical Scientist. You will hold an MSc, FIBMS or equivalent experience in a similar role, as well as experience of quality management. Familiarity with GMP regulations is also an advantage,
This role is vital to the clinical governance and risk management of the laboratory services you support. You will support the Quality Manager in ensuring these laboratory services are meeting ISO 15189 standards, MHRA requirements and in maintaining UKAS accreditation for each area. You will have a high level of responsibility to ensure the successful delivery of pathology services, in line with our corporate objectives.
The successful candidate will support the Quality Manager in oversight of the laboratory services Quality Management System (QMS) and for monitoring and developing this in line with the central Synnovis QMS. They will be involved in training of staff in QMS tasks including internal audit, document control and management of non-conformances.
All Synnovis services use QPulse as a quality management database, so experience in the use of this software will be valuable.
The role involves collating data for regular reports on the quality management system and which will include updates on key quality indicators and presenting these reports at governance meetings.
Supporting the laboratories with UKAS assessments is a key element of the role – this directing the laboratories in preparation for assessments; following up on any findings and ensuring evidence is available for submission to UKAS; and participating in assessments.
Your development and learning
You will have a suite of learning opportunities available through The Synnovis Way Development programme, the Scientific Learning and Development Fund and the Synnovis Academy through which you can receive funding / support for advanced qualifications.
The Synnovis Quality Team work together to constantly share learning and experience, either through regular group meetings or on a one-to-one basis. This provides a supportive and instructive environment to develop quality management skills.
At Synnovis, we are currently shaping the future of pathology services by creating a world-leading Hub and Spoke pathology network with our NHS partners. A large part of this modernisation will involve moving 70% of our services to a purpose built, state of the art Hub laboratory in the heart of London. For now, the job you are applying for will be based at one of our hospital sites however, from 1 April 2024 our people and services will start to move to our Hub laboratory in Blackfriars, Southwark, SE1, with some work remaining in refurbished essential services laboratories across our hospital network, focusing on the rapid turnover of urgent tests. Please do ask your recruiting manager if you wish to find out more.

You will hold a variety of accountabilities in the laboratory environment. These include, but are not limited to:

  • Contribute to the ongoing delivery of quality management through the Quality Management System (QMS), supporting the Quality Managers as required.
  • Collate information and compile Quality reports.
  • Support the introduction of new analysers/assays/methodologies by identifying and advising on any quality related aspects, improving patient pathways and service delivery.
  • Take part in activities such as audits, investigations, incidents and quality assurance.
  • Support and lead on quality related training for all laboratory employees in your area.
  • Deputise for the Quality Manager including attendance at meetings, as required
  • Ensure compliance with all regulatory and quality requirements of regulatory directives, accreditation bodies, and local management including:
  • Care Quality Commission

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Hospital/Health Care

Pharma / Biotech / Healthcare / Medical / R&D

Health Care

Graduate

Proficient

1

London SE1 8NZ, United Kingdom