Clinical Laboratory Lead
2025-08-29T20:39:02+00:00
Zambart
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FULL_TIME
Lusaka
Lusaka
10101
Zambia
Healthcare
Healthcare
2025-09-05T17:00:00+00:00
Zambia
8
Key Responsibilities include and not limited to
1. Leadership & Management
- Lead and coordinate clinical laboratory operations across studies.
- Create and manage team schedules to ensure adequate coverage and efficiency.
- Lead regular lab management meetings to review operations, quality issues, and team performance.
- Serve as the primary liaison between Zambart and external institutions, regulatory bodies, and health authorities.
- Ensure adherence to safety, good housekeeping, and ethical standards, including participant confidentiality.
2. Laboratory Certification and Accreditation
- Lead Zambart’s application process for SADCAS accreditation
- Develop and implement a clear SADCAS accreditation roadmap with timelines, milestones, and measurable targets.
- Coordinate gap assessments and ensure corrective actions are implemented to meet ISO 15189:2022 requirements.
- To follow through with the HPCZ certification process
- Work closely with laboratory staff to implement and monitor compliance with the Quality Management System (QMS)
- Responsible for organizing, coordinating, and documenting all Internal Quality Assurance (IQA) and External Quality Assurance (EQA) programs
- Coordinate, develop and review standard operating procedures (SOPs), monitor compliance, and maintain records and documentation
- Develop, present, and document quality assurance (QA) training programs for laboratory staff
- Maintain databases and computer programs for the compilation and statistical analysis of quality assurance (QA) data
- Maintain and update records of laboratory equipment, maintenance, and service in accordance with ISO 15189:2022
- Hold weekly meetings at lab management level to review quality issues
3. Technical Oversight and Data Quality in the Clinical Unit
- Manage workflows and coordinate laboratory activities for the clinical laboratory unit
- Creating and managing team schedules in the clinical unit
- Design systematic plans of action for problem solving as a build-up to practical and timely decision-making
- Ensure proper adherence by lab staff to regulations as required by research ethics and public health guidelines
- Laboratory data validation for all studies and ensuring results released are of high quality with acceptable turnaround time
- Routine reviewing of laboratory equipment monitoring logs
- Develop and maintain appropriate working relationships between Zambart and client institutions and health authorities
- Coordinating sample transportation between collection site and laboratory
- Participate in and supervise sample testing to guarantee accurate and reliable results
- Monitoring and reviewing data entry procedures for laboratory databases
- Reviewing laboratory supplies reports inventory, monitoring stocks of laboratory supplies and reagents, preventing shortages
- Ensure that ethical guidelines are always adhered to concerning confidentiality of participant and project data and information
- Ensuring safety and good housekeeping standards in the laboratory (or designated unit) are in place and adhered to
- Participate in writing and updating laboratory SOPs, and ensure proper adherence to policies and SOPs
- Attend scientific meetings and conferences to stay updated on industry developments
- Maintain and update professional knowledge, taking responsibility for continuing professional development (CPD)
- Be willing to work flexible hours, including late hours or weekends when required
- Perform any other duties or responsibilities deemed necessary by the organization to ensure efficient and timely implementation of lab operations
QUALIFICATIONS AND EXPERIENCE
Essential Requirements:
- Minimum BSc Biomedical Sciences
- Minimum 5 years’ experience in a clinical or research laboratory setting
- Experience working in a laboratory that has been accredited
- Strong interpersonal and team leadership skills.
Desirable:
- At least 2 years in a leadership role.
- Experience in developing a laboratory for accreditation with ISO 15189:2022, HPCZ certification, and QMS implementation.
1. Leadership & Management Lead and coordinate clinical laboratory operations across studies. Create and manage team schedules to ensure adequate coverage and efficiency. Lead regular lab management meetings to review operations, quality issues, and team performance. Serve as the primary liaison between Zambart and external institutions, regulatory bodies, and health authorities. Ensure adherence to safety, good housekeeping, and ethical standards, including participant confidentiality. 2. Laboratory Certification and Accreditation Lead Zambart’s application process for SADCAS accreditation Develop and implement a clear SADCAS accreditation roadmap with timelines, milestones, and measurable targets. Coordinate gap assessments and ensure corrective actions are implemented to meet ISO 15189:2022 requirements. To follow through with the HPCZ certification process Work closely with laboratory staff to implement and monitor compliance with the Quality Management System (QMS) Responsible for organizing, coordinating, and documenting all Internal Quality Assurance (IQA) and External Quality Assurance (EQA) programs Coordinate, develop and review standard operating procedures (SOPs), monitor compliance, and maintain records and documentation Develop, present, and document quality assurance (QA) training programs for laboratory staff Maintain databases and computer programs for the compilation and statistical analysis of quality assurance (QA) data Maintain and update records of laboratory equipment, maintenance, and service in accordance with ISO 15189:2022 Hold weekly meetings at lab management level to review quality issues 3. Technical Oversight and Data Quality in the Clinical Unit Manage workflows and coordinate laboratory activities for the clinical laboratory unit Creating and managing team schedules in the clinical unit Design systematic plans of action for problem solving as a build-up to practical and timely decision-making Ensure proper adherence by lab staff to regulations as required by research ethics and public health guidelines Laboratory data validation for all studies and ensuring results released are of high quality with acceptable turnaround time Routine reviewing of laboratory equipment monitoring logs Develop and maintain appropriate working relationships between Zambart and client institutions and health authorities Coordinating sample transportation between collection site and laboratory Participate in and supervise sample testing to guarantee accurate and reliable results Monitoring and reviewing data entry procedures for laboratory databases Reviewing laboratory supplies reports inventory, monitoring stocks of laboratory supplies and reagents, preventing shortages Ensure that ethical guidelines are always adhered to concerning confidentiality of participant and project data and information Ensuring safety and good housekeeping standards in the laboratory (or designated unit) are in place and adhered to Participate in writing and updating laboratory SOPs, and ensure proper adherence to policies and SOPs Attend scientific meetings and conferences to stay updated on industry developments Maintain and update professional knowledge, taking responsibility for continuing professional development (CPD) Be willing to work flexible hours, including late hours or weekends when required Perform any other duties or responsibilities deemed necessary by the organization to ensure efficient and timely implementation of lab operations
Minimum BSc Biomedical Sciences Minimum 5 years’ experience in a clinical or research laboratory setting Experience working in a laboratory that has been accredited Strong interpersonal and team leadership skills.
JOB-68b20fe6a0d70
Vacancy title:
Clinical Laboratory Lead
[Type: FULL_TIME, Industry: Healthcare, Category: Healthcare]
Jobs at:
Zambart
Deadline of this Job:
Friday, September 5 2025
Duty Station:
Lusaka | Lusaka | Zambia
Summary
Date Posted: Friday, August 29 2025, Base Salary: Not Disclosed
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JOB DETAILS:
Key Responsibilities include and not limited to
1. Leadership & Management
- Lead and coordinate clinical laboratory operations across studies.
- Create and manage team schedules to ensure adequate coverage and efficiency.
- Lead regular lab management meetings to review operations, quality issues, and team performance.
- Serve as the primary liaison between Zambart and external institutions, regulatory bodies, and health authorities.
- Ensure adherence to safety, good housekeeping, and ethical standards, including participant confidentiality.
2. Laboratory Certification and Accreditation
- Lead Zambart’s application process for SADCAS accreditation
- Develop and implement a clear SADCAS accreditation roadmap with timelines, milestones, and measurable targets.
- Coordinate gap assessments and ensure corrective actions are implemented to meet ISO 15189:2022 requirements.
- To follow through with the HPCZ certification process
- Work closely with laboratory staff to implement and monitor compliance with the Quality Management System (QMS)
- Responsible for organizing, coordinating, and documenting all Internal Quality Assurance (IQA) and External Quality Assurance (EQA) programs
- Coordinate, develop and review standard operating procedures (SOPs), monitor compliance, and maintain records and documentation
- Develop, present, and document quality assurance (QA) training programs for laboratory staff
- Maintain databases and computer programs for the compilation and statistical analysis of quality assurance (QA) data
- Maintain and update records of laboratory equipment, maintenance, and service in accordance with ISO 15189:2022
- Hold weekly meetings at lab management level to review quality issues
3. Technical Oversight and Data Quality in the Clinical Unit
- Manage workflows and coordinate laboratory activities for the clinical laboratory unit
- Creating and managing team schedules in the clinical unit
- Design systematic plans of action for problem solving as a build-up to practical and timely decision-making
- Ensure proper adherence by lab staff to regulations as required by research ethics and public health guidelines
- Laboratory data validation for all studies and ensuring results released are of high quality with acceptable turnaround time
- Routine reviewing of laboratory equipment monitoring logs
- Develop and maintain appropriate working relationships between Zambart and client institutions and health authorities
- Coordinating sample transportation between collection site and laboratory
- Participate in and supervise sample testing to guarantee accurate and reliable results
- Monitoring and reviewing data entry procedures for laboratory databases
- Reviewing laboratory supplies reports inventory, monitoring stocks of laboratory supplies and reagents, preventing shortages
- Ensure that ethical guidelines are always adhered to concerning confidentiality of participant and project data and information
- Ensuring safety and good housekeeping standards in the laboratory (or designated unit) are in place and adhered to
- Participate in writing and updating laboratory SOPs, and ensure proper adherence to policies and SOPs
- Attend scientific meetings and conferences to stay updated on industry developments
- Maintain and update professional knowledge, taking responsibility for continuing professional development (CPD)
- Be willing to work flexible hours, including late hours or weekends when required
- Perform any other duties or responsibilities deemed necessary by the organization to ensure efficient and timely implementation of lab operations
QUALIFICATIONS AND EXPERIENCE
Essential Requirements:
- Minimum BSc Biomedical Sciences
- Minimum 5 years’ experience in a clinical or research laboratory setting
- Experience working in a laboratory that has been accredited
- Strong interpersonal and team leadership skills.
Desirable:
- At least 2 years in a leadership role.
- Experience in developing a laboratory for accreditation with ISO 15189:2022, HPCZ certification, and QMS implementation.
Work Hours: 8
Experience in Months: 60
Level of Education: bachelor degree
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