Biomedical Engineer
2025-10-02T09:00:43+00:00
Pharmacy and Poisons Board
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FULL_TIME
Kenya
Nairobi
00100
Kenya
Public Administration, and Government
Health Professionals
2025-10-15T17:00:00+00:00
Kenya
8
Job Purpose
The position is responsible for the day-to-day regulatory activities of implementing standards, procedures, and guidelines to ensure the quality, safety, and efficacy of health products and technologies, and that pharmacy professionals are competent and fit to practice.
Buy vitamins and supplements
Duties and Responsibilities
- Support implementation of guidelines, standards, infrastructure, procedures, and tools for medical devices
- Support implementation of quality management systems and risk-benefit strategies regarding quality systems requirements for medical devices, risk management principles, and ISO 13485 standards
- Compile a list of Medical Devices and In-Vitro Diagnostics recommended for granting, withdrawal, suspension, renewal, and revocation of marketing authorization
- Maintain a register of all authorized Medical Devices and In-Vitro Diagnostics
- Participate in publishing lists of authorized or registered Medical Devices and In-Vitro Diagnostics with marketing authorizations
- Implement international guidelines, standards, and tools for post-market surveillance, risk management, advertising and promotional regulations, and supervision of reprocessing single-use medical devices
- Evaluate applications for marketing authorization of Medical Devices and In-Vitro Diagnostics supplied to the public
- Recommend the list of Medical Devices and In-Vitro Diagnostics approved for export
- Participate in capacity development programs related to evaluation, registration, retention, and renewal of Medical Devices and In-Vitro Diagnostics
Person Specifications
For appointment to this grade, a candidate must:
- Have a Bachelor’s Degree in Biomedical Engineering or other health science degree or its equivalent qualification from a recognized institution
- Experience in regulation of medical devices and In-Vitro Diagnostics will be an added advantage
- Hold a professional qualification and membership to a professional body, where applicable
- Be proficient in computer knowledge and skills
- Have good analytical and communication skills
- Fulfil the requirements of Chapter Six of the Constitution
Support implementation of guidelines, standards, infrastructure, procedures, and tools for medical devices
Support implementation of quality management systems and risk-benefit strategies regarding quality systems requirements for medical devices, risk management principles, and ISO 13485 standards
Compile a list of Medical Devices and In-Vitro Diagnostics recommended for granting, withdrawal, suspension, renewal, and revocation of marketing authorization
Maintain a register of all authorized Medical Devices and In-Vitro Diagnostics
Participate in publishing lists of authorized or registered Medical Devices and In-Vitro Diagnostics with marketing authorizations
Implement international guidelines, standards, and tools for post-market surveillance, risk management, advertising and promotional regulations, and supervision of reprocessing single-use medical devices
Evaluate applications for marketing authorization of Medical Devices and In-Vitro Diagnostics supplied to the public
Recommend the list of Medical Devices and In-Vitro Diagnostics approved for export
Participate in capacity development programs related to evaluation, registration, retention, and renewal of Medical Devices and In-Vitro Diagnostics
Be proficient in computer knowledge and skills
Have good analytical and communication skills
Fulfil the requirements of Chapter Six of the Constitution
Have a Bachelor’s Degree in Biomedical Engineering or other health science degree or its equivalent qualification from a recognized institution
Experience in regulation of medical devices and In-Vitro Diagnostics will be an added advantage
Hold a professional qualification and membership to a professional body, where applicable
JOB-68de3f3b1798e
Vacancy title:
Biomedical Engineer
[Type: FULL_TIME, Industry: Public Administration, and Government, Category: Health Professionals]
Jobs at:
Pharmacy and Poisons Board
Deadline of this Job:
Wednesday, October 15 2025
Duty Station:
Kenya | Nairobi | Kenya
Summary
Date Posted: Thursday, October 2 2025, Base Salary: Not Disclosed
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JOB DETAILS:
Job Purpose
The position is responsible for the day-to-day regulatory activities of implementing standards, procedures, and guidelines to ensure the quality, safety, and efficacy of health products and technologies, and that pharmacy professionals are competent and fit to practice.
Buy vitamins and supplements
Duties and Responsibilities
- Support implementation of guidelines, standards, infrastructure, procedures, and tools for medical devices
- Support implementation of quality management systems and risk-benefit strategies regarding quality systems requirements for medical devices, risk management principles, and ISO 13485 standards
- Compile a list of Medical Devices and In-Vitro Diagnostics recommended for granting, withdrawal, suspension, renewal, and revocation of marketing authorization
- Maintain a register of all authorized Medical Devices and In-Vitro Diagnostics
- Participate in publishing lists of authorized or registered Medical Devices and In-Vitro Diagnostics with marketing authorizations
- Implement international guidelines, standards, and tools for post-market surveillance, risk management, advertising and promotional regulations, and supervision of reprocessing single-use medical devices
- Evaluate applications for marketing authorization of Medical Devices and In-Vitro Diagnostics supplied to the public
- Recommend the list of Medical Devices and In-Vitro Diagnostics approved for export
- Participate in capacity development programs related to evaluation, registration, retention, and renewal of Medical Devices and In-Vitro Diagnostics
Person Specifications
For appointment to this grade, a candidate must:
- Have a Bachelor’s Degree in Biomedical Engineering or other health science degree or its equivalent qualification from a recognized institution
- Experience in regulation of medical devices and In-Vitro Diagnostics will be an added advantage
- Hold a professional qualification and membership to a professional body, where applicable
- Be proficient in computer knowledge and skills
- Have good analytical and communication skills
- Fulfil the requirements of Chapter Six of the Constitution
Work Hours: 8
Experience in Months: 24
Level of Education: bachelor degree
Job application procedure
interested applicant please, Click here to apply
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