Genomic Sequencing Research Scientist (SOG/ST 7)

Organisation
Ministry of Health and Wellness
Reference
VAC-65912
Contract Type
Full-Time
Industries
Scientific
Location
Kingston
Salary & Benefits
$5,198,035.00 per annum
Date Posted
02/09/2026
Expiry Date
18/09/2026
The incumbent conducts experiments, processes samples, maintains equipment and inventory, and documents data to support genomic sequencing and research operations under senior guidance.

 

JOB PURPOSE

Reporting to the Manager, National Genomic Sequencing Facility the Genomic Sequencing Research Scientist is required to perform scientific/technical activities at the National Genomic Sequencing Facility (NGSF) to inform and support patient care decisions and treatment in accordance with the Ministry's objectives.

The ideal candidate should have a background in genomics, molecular biology with a passion for advancing our understanding of genetics in both human health and disease. The incumbent will work on projects involving the analysis of genomic data, contribute to the development of novel research tools, and collaborate with the different laboratory teams to push the frontiers of national genomics research.

 

KEY OUTPUTS:

  • Specimens received in department processed according to standard operating procedures
  • Reports prepared and submitted to the supervisor
  • Protocols developed and updated
  • Monthly, annual and special Key Performance Indicators data, collected, collated and submitted
  • Monitor reagents, consumables and supplies inventory
  • Equipment, Reagent and Consumables inventory created and maintained
  • Sample filing system designed and monitored
  • Quality program monitored and appropriate corrective and preventive action performed
  • Sample filing system designed and monitored
  • Result database updated and maintained
  • Individual work plan developed

 

KEY RESPONSIBILITY AREAS

Management/Administrative Responsibilities

  • Manages the ordering and maintenance of reagents and consumables for optimal performance of all laboratory work
  • Attends monthly/quarterly/annual meetings, conferences, workshops, and special sessions (international and local) as required
  • Participates in the selection of new laboratory instruments and the development of new technologies to enable improved and more efficient service
  • Prepares data for weekly/monthly/annual reports or updates
  • Prepares individual work plan

Technical Responsibilities

  • Conducts laboratory experiments and tests based on established protocols or under the guidance of senior scientists
  • Performs routine and complex laboratory procedures such as preparing reagents, conducting assays, and maintaining laboratory equipment
  • Collects, processes, and analyzes samples (e.g., blood, tissue, water, environmental samples, etc.) to generate reliable data National Genomic Sequencing Facility/Job Description/Created May 2026
  • Maintains proper documentation of all laboratory procedures and data, following appropriate protocols and regulatory guidelines
  • Records and documents experimental results, ensuring all data is accurate, complete, and properly organized
  • Designs and maintains laboratory procedures, protocols and other documents related to Genomic Sequencing technologies
  • Ensures laboratory equipment is maintained and calibrated properly, troubleshooting issues as needed
  • Monitors inventory levels of laboratory supplies and manages ordering and stock maintenance, ensuring proper storage and handling of chemicals and reagents
  • Adheres to safety protocols and regulatory requirements, maintaining a safe and compliant lab environment
  • Assists with the design, planning, and execution of laboratory experiments
  • Prepares and reviews reports and presentations based on experimental results for internal and external stakeholders
  • Interprets and communicates research findings, including preparing reports, publications, and presentations for academic and industry stakeholders
  • Collaborates with team members and other departments to support ongoing research and testing initiatives
  • Conducts literature reviews and supports the writing of research reports and publications

 

PERFORMANCE STANDARDS

  • All specimens received in department processed according to standard operating procedures within the established timeline
  • Reports prepared are accurate and submitted within the agreed guidelines and timeline
  • Protocols developed and updated within the agreed timeline
  • Monthly, Annual and Special Key Performance Indicators data, collected, collated and submitted and appropriate corrective and preventive action performed within the agreed timeline
  • Reagents, consumables and supplies inventory monitored, and report submitted according to guidelines and within specified timeframe
  • Equipment, reagent and consumables inventory created and maintained according to guidelines
  • Sample filing system designed and monitored according to established schedule
  • Quality program monitored and appropriate corrective and preventive action performed within established timeframe
  • Sample filing system designed and monitored and reviewed within agreed timeframe
  • Result database updated and maintained according to established guidelines and within given timeframe
  • Individual work plan developed and submitted within the agreed timeline

 

TECHNICAL COMPETENCIES

  • Analytical and report writing skills
  • Sound knowledge in the principles of quality assurance techniques
  • Knowledge of standard laboratory techniques and procedures
  • Knowledge of the care and preservation of specimens
  • Knowledge of the operation, care and maintenance of laboratory equipment
  • Use of technology- relevant computer applications such as Microsoft Office Suite
  • Ability to perform laboratory procedures for extended periods
  • Knowledge of the Public Health Laws and Regulations
  • Ability to perform pre-analytical, analytical, and post-analytical phases of testing

 

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • Bachelor's degree in Scientific disciplines such as Biology, Microbiology, Biochemistry, or a related field.
  • Five (5) years' Clinical Laboratory experience, two (2) of which should be in the area of Virology, Molecular Microbiology or Immunology.
  • Knowledge of Laboratory Quality Management Systems
  • Experience with laboratory safety procedures and compliance standards
  • Certification and extensive knowledge in Medical and Testing Laboratory guidelines such as GLP (Good Laboratory Practice), ISO 15189, ISO15190, ISO 17025 and ISO9001.

 

 

 

 

 

The Ministry of Health & Wellness thanks all applicants for their interest; however, please note that only short-listed candidates will be contacted.

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