Superna Kaur Sohal Email & Phone Number

United Kingdom

London, England, United Kingdom

- Main point of contact for the site as a Quality Assurance Manager. - Provide support for affiliated field clinical laboratories in Africa and Europe and for current HIL and IAVI clinical trials. - Provide leadership, activity in a regulated (GxP) environment.

Oxford, United Kingdom

- Quality Assurance Manager for UK Oxford responsibilities held to ensure that the Lab is fit for purpose, and meets both external and internal requirements, legal compliance and meet customers expectations. - Managed the Somascan services/ assay by reviewing and releasing study data and associated study information. Manage the non-conformance and CAPA where related to Somascan studies and batch record for root cause analysis. - Managed equipment history files and maintain the calibration records. - Worked alongside with the US team to harmonise policies and procedures.

London, United Kingdom

- Ensured compliance with requirements of external Quality Assurance schemes and that all internal Quality Assurance is monitored to meet the requirement of ISO 15189. - Monitored the functioning and effectiveness of the Quality Management system, make recommendations for improvement and work with Senior Managers to develop and implement action plans.- Guaranteed the implementation of Trust, Directorate and Departmental policies, procedures and standards as agreed by the Trust Board, Pathology Operations Team and Departmental Management Team, Monitoring and following up on any issues of non-compliance.- Took a consistent and proactive approach to reduction of clinical risk, to promote clinical effectiveness and a safe and healthy environment in line with the Quality strategy. - Worked with the Pathology Quality & Governance Manager and local Clinical Governance leads to develop and implement initiatives to resolve clinical governance issues within Pathology. - Facilitate quarterly risk assessments across all Laboratories in conjunction with site managers and senior clinical staff, maintaining and updating the Directorate Risk Register appropriately - ensuring the appropriate follow up and action plans are in place and report progress/developments in management action for presentation to the Departmental Management. - Followed up on external assessments (UKAS, MHRA, Public Health England PHE) and verify the completion of corrective actions as required by the assessor’s report. - Planned, conducted and supervised a program of internal audits against defined quality performance measures and standards ensuring that effective immediate and follow up actions are completed.

Heston, Middlesex Tw5 9Qa

- First line manager for the Semi-Automation Department consisting Global, Regional and Local Clinical Trials assay's in Hematology, Flow Cytometry, Microbiology, Immunology and Molecular Biology and a member of the Quality Improvement Team.- Responsible for writing and updating departmental practiced related SOP's.Regulatory/ Compliance experiences in auditing and CAPA responses.

Heston, England

- Quality Assurance (QA): Preparation and delivering of QA metrics to the monthly management meetings to Consultants and Senior Leadership Team.- Training and Competency: Trained, Mentored and supervised staff in all processes within department- Work Management: Supervised the day-to-day running of the department ensuring client metrics such as Turnaround Times were met.- Troubleshooting: Supervisory level training on troubleshooting all analyzers within the department.- Auditing: Managed Regulatory (MHRA, CPA, CAP, ISO) and Client (GSK,Merck,Pfizer) specific audits.

Heston, Middlesex Tw5 9Qa

- Quality Assurance (QA): Preparation and delivering of QA metrics to the monthly management meetings.- Training and Competency: Trained, Mentored and supervised staff in all processes within department.- Work Management: Supervised the day-to-day running of the department ensuring client metrics.- Troubleshooting: Supervisory level training on troubleshooting all analyzers within the department.- Auditing: successfully managed Regulatory (MHRA, CPA, CAP, ISO) and client (GSK,Merck,Pfizer) specific audits.

Hammersmith,London

- Performed the day-to-day processing of samples as a Biomedical Scientist in Haematology and Blood Transfusion. - Trained new starters and junior members of the team in the Haematology department included Coagulation and the management of anticoagulant patient clinics.

Essex Ig1 ,London

Trainee Biomedical Scientist working towards HCPC registration in Haematology and Blood Transfusion.