QC Supervisor (Lab) in Hammersmith

We are a leading Genetic Testing organisation seeking an experienced Laboratory Supervisor (Biomedical Scientist) to join our team on a permanent, full-time basis in our Hammersmith Laboratory, London. This is an excellent opportunity to join a rapidly growing BioTech company and to share in our success as we grow.

You will be responsible for carrying out patient testing and reporting within the London laboratory alongside the supervision of existing staff to provide comprehensive, modern, high quality Clinical Genetics services to both private and NHS patients.

In addition, the post holder will support the Quality Management System and processes and support in maintaining existing accreditation under ISO 15189 and certification under ISO 13485, in addition to undertaking the scientific duties and responsibilities of a Lab supervisor/Biomedical Scientist.

• To provide Laboratory testing and interpretation of the results from highly complex diagnostic techniques (NGS/QPCR) that contribute to patient diagnostics and management.
• To maintain an accurate record of the work undertaken, including both manual and computerised records.
• Maintain and develop appropriate competency and expertise in scientific and technical areas.
• To manage staff in running the genetic diagnostic service.
• To conduct data analysis, ensuring the validity and reliability of data at all times.
• To be competent in the writing, implementation and closure of SOPs/NCRs/CAPA and Change Controls as well as supporting the corporate and Laboratory QMS.
• To ensure laboratory compliance for both testing and equipment regulations and requirements.
• Participate in research and development projects as required.

Requirements:

• BSc in Biomedical Science degree or equivalent.
• MSc in Biomedical Sciences or equivalent post graduate qualification/experience.
• Several years’ experience providing diagnostic DNA sequencing laboratory services (Ideally in a commercial Laboratory).
• Good knowledge of Medical laboratories Requirements (ISO 15189).
• Core molecular biology techniques relating to DNA studies.
• Great communication skills and leadership qualities to empower the team in a complex and busy department – proven managerial experience.
• Clear, concise report writing skills including strategy documents, briefings.
• Ability and willingness to travel between campuses.
• The ability swiftly to assimilate and synthesise new information using databases.
• Flexible attitude towards working hours.
• An understanding of genome annotation and the use of web-based browsers to interrogate genomic information.
• Knowledge of the genetic basis of human disease.
• Association of Clinical Biochemists or Clinical Genetics Society.
• Study on a management course or working towards a recognised management qualification.
• Good knowledge of UK, ISO and EU regulations for In-Vitro Diagnostics Devices, Medical Devices, and healthcare; State registration with the HCPC as a Biomedical Scientist.
• Have knowledge of departmental IT systems, EQMS, LIMs and appropriate automated software packages.
• Minimum of 5 years Lab Based Experience Required.
• Good level of understanding in relation to Quality and Regulatory policies and procedures required in a lab setting.
• Work effectively, independently and under supervision, being able to adapt to fast pace rapidly changing environment.
• Must demonstrate sound judgment, analytical skills to enable assessment of risk.
• Investigational and problem-solving skills – root cause analysis.
• Create and maintain a high-quality image of the company in front of different stakeholders.
• Fluent in English (oral and written) main language used within the company for internal communications and QMS documents.

25 Days Holiday + Statutory days. Company Pension. Annual Salary Review and Performance Related Bonus.