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Pathologist

AVMLabs (Formerly Thyrocare Gulf Laboratories)

Riyadh

On-site

SAR 120,000 - 180,000

Full time

12 days ago

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Job summary

An established industry player in healthcare is seeking a skilled Pathologist to oversee laboratory operations. This role involves ensuring compliance with health regulations, maintaining quality standards, and managing a diverse team. The ideal candidate will have a strong educational background in Clinical Pathology and experience in managing accredited laboratories. This position offers flexible working options and the opportunity to work within a reputable brand in the healthcare sector, contributing to impactful patient care and innovation in laboratory practices.

Benefits

Flexible working options
Solid track record of performance
Reputable brand in healthcare

Qualifications

  • PhD, MD or Masters in Clinical and Chemical Pathology required.
  • Experience in managing accredited laboratories is essential.

Responsibilities

  • Oversee laboratory operations and ensure compliance with regulations.
  • Manage quality control processes and ensure accurate test results.

Skills

Effective communication skills
In-depth knowledge of laboratory best practices
Proficiency in laboratory software
Leadership qualities
Familiarity with safety protocols

Education

PhD in Clinical Pathology
MD in Clinical Pathology
Masters in Clinical and Chemical Pathology

Tools

Laboratory software
Data analysis tools

Job description

Preventive Healthcare Lab | Diagnostic Centre - AVMLabs Visit www.avmlabs.com or call us on +973 6600 4000 to book your next blood, serum, stool etc test at your home.

The Role

Job Title: Pathologist

Job Summary: Oversee and manage all aspects of laboratory operations, ensuring compliance with regulations, and maintaining quality standards. While there is room for delegation of certain duties, the lab director maintains ultimate responsibility for ensuring the proper execution of all tasks.

Duties and Responsibilities:
Daily Responsibility:

  • Verification that the IQC results are acceptable before patient testing. Follow up any trends in the patients results which may reflect a machine or specific analyte problem. Following up on corrective actions regarding customer complaints and providing preventive action for the repeated reasons.
Weekly Responsibility:
  • On weekly basis, the QC charts should be checked for presence of shifts or trends in the QC.
  • The QC charts should be checked again; the mean may need to be reset by verifying the current month trend with the cumulative mean. The CV% of each parameter to be verified and compared with manufacturer QC %CV as well as previous month CV%. Review the maintenance of the analyzers and temperature records. RIQAS and CAP results (if any) should be reviewed and recommend proper corrective action in case of unacceptable results.
Other Routine Responsibility:
  • Ensure effective Quality Management System (QMS) for the laboratory. Ensure the physical and environmental conditions of the laboratory are adequate and appropriate for the testing performed. The environment for employees is safe from physical, chemical, and biological hazards and safety and biohazard requirements are followed. Adequately educated, experienced, and/or trained personnel who provide appropriate consultation, supervise, and accurately perform tests and report test results in accordance with the written duties and responsibilities are employed by the laboratory. Each employee’s responsibilities and duties are specified in writing.
  • Ensure that the laboratory develops and uses a quality system approach to laboratory testing that provides accurate and reliable patient test results including:
  • Ongoing monitoring of each testing process in order to identify errors or potential problems that could result in errors.
  • Taking corrective action; and evaluating the corrective actions taken to make sure that they were effective and will prevent recurrence.
  • Consultations concerning test results and interpretation of those results as they relate to specific patient conditions. Appointing general supervisor to provide day-to-day supervision of all testing personnel and reporting of test results as well as provide on-site supervision for training of new staff. Adequate method verification of all analytes according to the accrediting authority requirements. Enrollment of the laboratory in proficiency testing (PT) program for the tests performed as appropriate for the accrediting authorities; PT samples are tested in accordance with the program requirements and according to the available policy; PT results are returned within the time frames established by the PT program; PT reports are reviewed, and corrective action plans are followed when PT results are found to be unacceptable or unsatisfactory. Establish and approve Quality control program with annual review, new test procedures and SOPs are available and initially approved and then reviewed every two years. Ensures that personnel have been appropriately trained and demonstrate competency prior to testing patient specimen and training or continuing education needed for other staff are identified and provided. Apply all standards for local and international accreditation as required and ensure the ongoing application of those standards and preparing for accreditation when decision is taken for specific accreditation. Ensures a thorough interim self-inspection is performed, and all deficiencies are corrected in a timely manner.
Ideal Profile:
  • Qualification: PhD, MD or Masters in Clinical and Chemical Pathology
  • Professional Experience: Good experience in managing accredited laboratory as decided by management.
Skills Required:
  • Recognized license as per ministry’s requirement defined for the respective location. Effective communication skills for collaboration with team members. In-depth knowledge of laboratory best practices, safety protocols, and compliance regulations. Proficiency in laboratory software and data analysis tools. Familiarity with industry trends and emerging technologies. Excellent communication and interpersonal skills. Leadership qualities that inspire and motivate a diverse team.
Important Note:

Following a change in laboratory directorship, the new laboratory director approves the technical policies and procedures within three months of the change of directorship.

What's on Offer?
  • Flexible working options
  • Work in a company with a solid track record of performance
  • Join a well-known brand within Hospital / Health Care / Healthtech
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