Biotechnologist Specialist job at Pharmacy and Poisons Board
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Biotechnologist Specialist
2025-09-29T21:43:59+00:00
Pharmacy and Poisons Board
https://cdn.greatkenyanjobs.com/jsjobsdata/data/employer/comp_2627/logo/Pharmacy%20and%20Poisons%20Board,.png
FULL_TIME
 
Kenya
Nairobi
00100
Kenya
Public Administration, and Government
Science & Engineering
KES
 
MONTH
2025-10-14T17:00:00+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 implementation of Lot Release for vaccines and biotherapeutics registration.

Duties and Responsibilities:

  • Interpreting test data relative to established specifications, standards and control limits, and making recommendations on appropriateness
  • Ensuring all vendors are qualified and adhere to vendor qualification and performance standards
  • Reviewing test data from contract laboratories and external calibration service providers to ensure accuracy and regulatory compliance
  • Using statistical methods and applying business and economic data in decision-making
  • Identifying patterns in data indicating test system deviations and investigating/troubleshooting issues
  • Establishing corrective and preventive actions and ensuring review and follow-up
  • Executing and approving/closing-out laboratory investigations
  • Systematically reviewing operational procedures to identify risks and areas for improvement
  • Reviewing lot summary protocols and recommending approval of lot release certificates
  • Conducting and documenting regular safety inspections
  • Ensuring compliance with organizational and regulatory Health and Safety Policies
  • Establishing waste management programmes for hazardous, biological, pharmaceutical, and chemical waste
  • Ensuring analytical reports comply with standards and regulations
  • Verifying analytical reports produced by other analysts
  • Developing, installing, and revising validation procedures and protocols
  • Writing and reviewing technical reports including deviation reports and testing protocols
  • Coordinating and tracking projects
  • Training project teams and reporting performance metrics
  • Developing and maintaining project timelines and resource plans
  • Ensuring integration of quality control functions with other regulatory functions
  • Evaluating performance of analytical methods and procedures
  • Investigating or reporting questionable or aberrant test results
  • Monitoring testing procedures to ensure compliance with established specifications
  • Preparing high-quality documents including experimental protocols and technical reports
  • Overseeing equipment calibration, qualification, maintenance, and troubleshooting
  • Performing and interpreting standard, complex, and specialized tests
  • Researching, developing, implementing, and evaluating new methodologies

Person Specifications:
For appointment to this grade, a candidate must:

  • Have a Bachelor's Degree in Pharmacy, Biotechnology, Biochemistry, Molecular Biology, Microbiology, Biomedical Engineering or equivalent qualification
  • Have at least eight (8) years relevant work experience, three (3) of which must have been in a supervisory role
  • Master's Degree in Biotechnology, Vaccinology, Biotherapeutics, Immunology, or related field is an added advantage
  • Certified courses in Biologics Development and Manufacturing or vaccines manufacturing
  • Professional certification and membership with a relevant professional body
  • Certificate in management course lasting not less than four (4) weeks
  • Be proficient in computer applications
  • Have demonstrated merit and ability as reflected in work performance and results
  • Fulfill the requirements of Chapter Six of the Constitution

Application Requirements:
Candidates must submit:

  • Detailed curriculum vitae
  • Academic transcripts and certificates
  • KRA PIN
  • NCPWD certificate (for persons with disability)
  • Passport photo

Important Notice:

  • Shortlisted candidates must submit clearance certificates from KRA, EACC, Credit Reference Bureau, and Kenya Police
  • Original certificates and national ID/passport must be presented
  • Providing false information is an offence
  • PPB does not charge any recruitment fees
  • PPB is an equal opportunity employer
  • Persons with disability, female candidates, and marginalized/minority groups are encouraged to apply
 
 
 
bachelor degree
96
JOB-68dafd9f5b364

Vacancy title:
Biotechnologist Specialist

[Type: FULL_TIME, Industry: Public Administration, and Government, Category: Science & Engineering]

Jobs at:
Pharmacy and Poisons Board

Deadline of this Job:
Tuesday, October 14 2025

Duty Station:
Kenya | Nairobi | Kenya

Summary
Date Posted: Monday, September 29 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 implementation of Lot Release for vaccines and biotherapeutics registration.

Duties and Responsibilities:

  • Interpreting test data relative to established specifications, standards and control limits, and making recommendations on appropriateness
  • Ensuring all vendors are qualified and adhere to vendor qualification and performance standards
  • Reviewing test data from contract laboratories and external calibration service providers to ensure accuracy and regulatory compliance
  • Using statistical methods and applying business and economic data in decision-making
  • Identifying patterns in data indicating test system deviations and investigating/troubleshooting issues
  • Establishing corrective and preventive actions and ensuring review and follow-up
  • Executing and approving/closing-out laboratory investigations
  • Systematically reviewing operational procedures to identify risks and areas for improvement
  • Reviewing lot summary protocols and recommending approval of lot release certificates
  • Conducting and documenting regular safety inspections
  • Ensuring compliance with organizational and regulatory Health and Safety Policies
  • Establishing waste management programmes for hazardous, biological, pharmaceutical, and chemical waste
  • Ensuring analytical reports comply with standards and regulations
  • Verifying analytical reports produced by other analysts
  • Developing, installing, and revising validation procedures and protocols
  • Writing and reviewing technical reports including deviation reports and testing protocols
  • Coordinating and tracking projects
  • Training project teams and reporting performance metrics
  • Developing and maintaining project timelines and resource plans
  • Ensuring integration of quality control functions with other regulatory functions
  • Evaluating performance of analytical methods and procedures
  • Investigating or reporting questionable or aberrant test results
  • Monitoring testing procedures to ensure compliance with established specifications
  • Preparing high-quality documents including experimental protocols and technical reports
  • Overseeing equipment calibration, qualification, maintenance, and troubleshooting
  • Performing and interpreting standard, complex, and specialized tests
  • Researching, developing, implementing, and evaluating new methodologies

Person Specifications:
For appointment to this grade, a candidate must:

  • Have a Bachelor's Degree in Pharmacy, Biotechnology, Biochemistry, Molecular Biology, Microbiology, Biomedical Engineering or equivalent qualification
  • Have at least eight (8) years relevant work experience, three (3) of which must have been in a supervisory role
  • Master's Degree in Biotechnology, Vaccinology, Biotherapeutics, Immunology, or related field is an added advantage
  • Certified courses in Biologics Development and Manufacturing or vaccines manufacturing
  • Professional certification and membership with a relevant professional body
  • Certificate in management course lasting not less than four (4) weeks
  • Be proficient in computer applications
  • Have demonstrated merit and ability as reflected in work performance and results
  • Fulfill the requirements of Chapter Six of the Constitution

Application Requirements:
Candidates must submit:

  • Detailed curriculum vitae
  • Academic transcripts and certificates
  • KRA PIN
  • NCPWD certificate (for persons with disability)
  • Passport photo

Important Notice:

  • Shortlisted candidates must submit clearance certificates from KRA, EACC, Credit Reference Bureau, and Kenya Police
  • Original certificates and national ID/passport must be presented
  • Providing false information is an offence
  • PPB does not charge any recruitment fees
  • PPB is an equal opportunity employer
  • Persons with disability, female candidates, and marginalized/minority groups are encouraged to apply

 

Work Hours: 8

Experience in Months: 96

Level of Education: bachelor degree

Job application procedure

Quick Guiding Steps:

  1. Access the application system Click to apply
  2. Complete all mandatory fields and upload required documents in PDF format
  3. Ensure all uploaded documents are appropriately named
  4. Click 'submit' and logout

 

All Jobs | QUICK ALERT SUBSCRIPTION

Job Info
Job Category: Health/ Medicine jobs in Kenya
Job Type: Full-time
Deadline of this Job: Tuesday, October 14 2025
Duty Station: Kenya | Nairobi | Kenya
Posted: 30-09-2025
No of Jobs: 10
Start Publishing: 30-09-2025
Stop Publishing (Put date of 2030): 30-09-2070
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