Back to jobs
Job in Kenya

Principal Pharmaceutical Analyst (Biologics & Biopharmaceutical)

National Quality Control Laboratory (NQCL) Kenya Full Time Posted 2026-10-27
AI job insight

AI job insight

See full AI guide

NQCL is recruiting a Principal Pharmaceutical Analyst in Nairobi to perform pharmaceutical quality-control work focused on biologics and biopharmaceuticals. The role covers laboratory procedures and standards, CAPA, data security, operations, equipment qualification, reporting, and supervision of laboratory staff.

  • Principal role with NQCL, a Ministry of Health state corporation.
  • Develop procedures and maintain WHO and ISO 17025 laboratory practices.
  • Oversee CAPA, data security, budgets, procurement, and daily laboratory operations.
Source Great Kenyan Jobs Salary Not enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.

Similar jobs

More roles you may want to review before you leave.
CountyNairobiCityNot specifiedContractFull TimePosted2026-10-27Close dateNot specifiedExperienceNot specifiedSourceGreat Kenyan JobsAddress00100, Nairobi, Kenya
principal pharmaceutical analystbiologics quality controlbiopharmaceutical testingpharmaceutical laboratoryNairobifull timepublic sectorlaboratory managementISO 17025securityPharmaceutical analystLaboratory manager

AI summary

NQCL is recruiting a Principal Pharmaceutical Analyst in Nairobi to perform pharmaceutical quality-control work focused on biologics and biopharmaceuticals. The role covers laboratory procedures and standards, CAPA, data security, operations, equipment qualification, reporting, and supervision of laboratory staff.

  • Principal role with NQCL, a Ministry of Health state corporation.
  • Develop procedures and maintain WHO and ISO 17025 laboratory practices.
  • Oversee CAPA, data security, budgets, procurement, and daily laboratory operations.
  • Qualify analytical equipment and prepare reagents, standards, and reference materials.
  • Supervise technicians and laboratory assistants and produce technical reports.
  • Closing date listed as 16 November 2026.
Use AI for this job

AI job guide

Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.

AI salary guide

Not enough public data

Not enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.

Can you qualify for this role?

  • UnclearRelated work experienceThe text mentions experience, but the exact level should be confirmed at source.
  • RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
  • PreferredPractical evidence in security, Pharmaceutical analyst, Laboratory managerThe tags and summary point to skills connected with this role.
  • RequiredAvailability to work in NairobiThe vacancy is associated with this location.
  • UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.

Documents to prepare

  • Likely requiredUpdated CV
  • Role specificCover letter or short employer message
  • OptionalProfessional references
  • Role specificAcademic or professional certificates
  • VerifyID or passport only after verifying the employer

Application tips for this job

  • Place your strongest Principal Pharmaceutical Analyst (Biologics & Biopharmaceutical) evidence in the first half of your CV.
  • In your cover letter or employer message, connect your experience to National Quality Control Laboratory (NQCL) and the role in Nairobi.
  • Add concrete examples related to security, Pharmaceutical analyst, Laboratory manager, ideally with measurable outcomes or clear responsibilities.
  • Follow the instructions from Great Kenyan Jobs; avoid sending documents to unofficial contacts or copied links.
  • Confirm the deadline, interview location and employer contact before sharing personal documents.
  • Prepare a polite question about pay, benefits and contract terms for later interview stages.

Source and safety check

  • Great Kenyan Jobs
  • Original source link available
  • Application method is clear
  • Deadline not specified
  • No major risk signal was detected in the captured text.

Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.

Interview preparation

  • What experience makes you a strong fit for this Principal Pharmaceutical Analyst (Biologics & Biopharmaceutical) role in security, Pharmaceutical analyst?
  • How have you handled responsibilities similar to those in this job post?
  • Are you available to work in Nairobi under the listed contract or schedule?
  • Prepare examples with clear responsibilities, tools used and measurable outcomes.
  • Review the source and research National Quality Control Laboratory (NQCL) before the interview.

Ask what the first priorities will be in the role and how success will be measured.

Original source description

Principal Pharmaceutical Analyst (Biologics & Biopharmaceutical)

2026-10-27T12:45:37+00:00

National Quality Control Laboratory

https://cdn.greatkenyanjobs.com/jsjobsdata/data/employer/comp_10909/logo/download%20(16).jpg

https://nqcl.go.ke/

FULL_TIME

Nairobi

Nairobi

00100

Kenya

Public Administration, and Government

Science & Engineering, Healthcare, Civil & Government, Professional Services

KES

MONTH

2026-11-16T17:00:00+00:00

8

National Quality Control Laboratory (NQCL) is a State Corporation within the Ministry of Health for Quality Control of Medicines on behalf of Government.

Job Specifications:

Duties and responsibilities at this level will entail;

Initiate the development and review of new procedures, guidelines in sample management;

Maintaining WHO good practices for Pharmaceutical Quality Control Laboratories and ISO 17025 standards;

Reviewing environmental control systems, investigating and issuing corrective and preventive action plans where necessary;

Communicating safety measures in the Laboratory and ensure availability of Safety Data Sheets (SDS) and avail each hazardous chemical;

Maintaining data security, protection and tracking through the Laboratory information system;

Undertaking performance management of the department including performance contracting and appraisal;

Participating in preparation of work plans and ensuring efficiency in the day-to-day operations of the Laboratory;

Generating requisition for approval and participate in departmental administrative plans including budgets and procurement plans;

Ensuring proper disposal of samples and reagents and Laboratory waste in accordance with all applicable procedures;

Performing routine and complex technical procedures and functions according to Standard Operating Procedures;

Participating in the resolution of client complaints relating to technical matters;

Updating records of recognized Reference materials including Chemical Reference substances, Buffer and cultures;

Participating in qualification of analytical equipment before commissioning and operating and troubleshooting instrumentation and perform preventive maintenance;

Preparing standard volumetric solutions and reagents following recognized formulas and experimental procedures;

Analyzing and recording test data to issue reports that use charts, graphs or narratives;

Supervising and instructing technicians and Laboratory Assistants;

Analyzing Out of Specification samples, radiopharmaceuticals and anti-cancers.

Capturing and updating relevant data and inventories for samples, reagents, microbes, solutions, equipment and animals related to testing and research of HPTs;

Participating in Laboratory Certificate Testing/ Inter-Laboratory Comparison (ILC) testing scheme and other activities for assuring quality of test results; and

Undertaking Continuous Professional Development in compliance with the regulatory requirements.

Person Specifications:

For appointment to this grade, an Officer must have:

Cumulative service period of nine (9) years’ relevant work experience, three (3) of which should have been at the grade of Senior Pharmaceutical Analyst or in a comparable position;

Bachelor’s Degree in Pharmacy, Environmental Health or equivalent qualification from a recognized Institution;

Certificate of Registration as a Pharmacist from Pharmacy and Poisons Board;

Membership to a relevant professional body;

Management Course not lasting less than four (4) weeks from a recognized institution;

Certificate in Occupational Safety and Health; and

Proficiency in computer application

Initiate the development and review of new procedures, guidelines in sample management

Maintaining WHO good practices for Pharmaceutical Quality Control Laboratories and ISO 17025 standards

Reviewing environmental control systems, investigating and issuing corrective and preventive action plans where necessary

Communicating safety measures in the Laboratory and ensure availability of Safety Data Sheets (SDS) and avail each hazardous chemical

Maintaining data security, protection and tracking through the Laboratory information system

Undertaking performance management of the department including performance contracting and appraisal

Participating in preparation of work plans and ensuring efficiency in the day-to-day operations of the Laboratory

Generating requisition for approval and participate in departmental administrative plans including budgets and procurement plans

Ensuring proper disposal of samples and reagents and Laboratory waste in accordance with all applicable procedures

Performing routine and complex technical procedures and functions according to Standard Operating Procedures

Participating in the resolution of client complaints relating to technical matters

Updating records of recognized Reference materials including Chemical Reference substances, Buffer and cultures

Participating in qualification of analytical equipment before commissioning and operating and troubleshooting instrumentation and perform preventive maintenance

Preparing standard volumetric solutions and reagents following recognized formulas and experimental procedures

Analyzing and recording test data to issue reports that use charts, graphs or narratives

Supervising and instructing technicians and Laboratory Assistants

Analyzing Out of Specification samples, radiopharmaceuticals and anti-cancers

Capturing and updating relevant data and inventories for samples, reagents, microbes, solutions, equipment and animals related to testing and research of HPTs

Participating in Laboratory Certificate Testing/ Inter-Laboratory Comparison (ILC) testing scheme and other activities for assuring quality of test results

Undertaking Continuous Professional Development in compliance with the regulatory requirements

Proficiency in computer application

Troubleshooting instrumentation

Preventive maintenance

Data security

Performance management

Budgeting

Procurement planning

Waste management

Client complaint resolution

Quality assurance

Bachelor’s Degree in Pharmacy, Environmental Health or equivalent qualification from a recognized Institution

Certificate of Registration as a Pharmacist from Pharmacy and Poisons Board

Membership to a relevant professional body

Management Course not lasting less than four (4) weeks from a recognized institution

Certificate in Occupational Safety and Health

bachelor degree

12

JOB-6ae09cf1828aa

Source and provenanceSource: Great Kenyan Jobs. Last checked: 2026-10-28.Kazi Connect is a job discovery service, not the employer. Always confirm the vacancy at the original source.Summaries may be AI-assisted. Report inaccurate content.
Never pay to apply. Always confirm the original source and watch for payment requests, sensitive document requests, or unrealistic promises.