Job Vacancies at Kairuki Pharmaceuticals Industry October 2026

Internship Level

Entry Level / Fresh Graduate

Key Learning Areas and Responsibilities

The QC Microbiology Intern will support the microbiology laboratory in activities related to pharmaceutical microbiological testing and environmental monitoring under appropriate supervision.

Responsibilities may include:

• Assisting in preparation of microbiological media and laboratory materials.
• Supporting microbiological testing of samples.
• Assisting with environmental monitoring activities.
• Supporting microbial limit and related microbiological tests.
• Assisting with laboratory cleaning and sanitization.
• Supporting sample collection and documentation.
• Maintaining laboratory records.
• Following Good Laboratory Practices (GLP) and GMP requirements.
• Supporting laboratory investigations under supervision.
• Maintaining proper laboratory safety and hygiene.

Qualifications

• Bachelor’s Degree in Microbiology, Biotechnology, Pharmacy, or a related field.
• Fresh graduates are encouraged to apply.
• Basic knowledge of microbiological laboratory techniques.
• Knowledge of pharmaceutical microbiology and environmental monitoring is an added advantage.
• Good laboratory and documentation skills.
• High attention to detail.
• Willingness to learn and work in a pharmaceutical manufacturing environment.

2: In-process Quality Assurance Intern

Key Learning Areas and Responsibilities

The intern will support the Quality Assurance team in monitoring manufacturing activities and ensuring compliance with approved quality systems.

Responsibilities may include:

• Supporting in-process monitoring activities.
• Assisting with review of manufacturing documentation.
• Supporting GMP compliance monitoring.
• Assisting with line clearance activities.
• Supporting documentation and record management.
• Participating in quality investigations under supervision.
• Supporting deviation and CAPA documentation.
• Assisting in monitoring production processes.
• Supporting QA personnel during inspections and audits.
• Learning pharmaceutical quality systems and GMP requirements.

Qualifications

• Bachelor’s Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, or a related field.
• Fresh graduates are encouraged to apply.
• Basic understanding of GMP and Quality Assurance principles.
• Good documentation and communication skills.
• High attention to detail.
• Willingness to learn and work in a pharmaceutical manufacturing environment.

3: Quality Control Chemistry Intern

Key Learning Areas and Responsibilities

The QC Chemistry Interns will support laboratory activities related to chemical and analytical testing of pharmaceutical materials and products under supervision.

Responsibilities may include:

• Assisting in preparation of laboratory reagents and solutions.
• Supporting analysis of raw materials, in-process materials, and finished products.
• Assisting with laboratory documentation and record keeping.
• Supporting testing using laboratory analytical techniques.
• Assisting with equipment preparation and cleaning.
• Supporting sample management and laboratory activities.
• Following Good Laboratory Practices (GLP) and GMP requirements.
• Maintaining laboratory cleanliness and safety.
• Supporting data recording and reporting.
• Learning pharmaceutical quality control procedures and analytical methods.

Qualifications

• Bachelor’s Degree in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or a related field.
• Fresh graduates are encouraged to apply.
• Basic knowledge of analytical chemistry and laboratory techniques.
• Knowledge of pharmaceutical quality control is an added advantage.
• Good analytical and documentation skills.
• High attention to detail.
• Ability to work effectively as part of a laboratory team.

4: Production Supervisors

Key Responsibilities

The Production Supervisors will oversee day-to-day manufacturing activities and ensure that production targets are achieved in accordance with approved procedures, GMP requirements, quality standards, and safety requirements.

Key responsibilities will include:

• Supervising daily production activities and production personnel.
• Ensuring production schedules and targets are achieved.
• Ensuring manufacturing processes are performed according to approved SOPs and batch manufacturing records.
• Supervising sterile IV pharmaceutical manufacturing activities.
• Ensuring compliance with Good Manufacturing Practices (GMP).
• Monitoring production processes and identifying deviations.
• Working closely with QA and QC to resolve quality and production issues.
• Ensuring proper documentation of production activities.
• Monitoring production equipment and reporting breakdowns promptly.
• Coordinating with Engineering for equipment maintenance.
• Managing production personnel and allocating duties effectively.
• Monitoring production performance and productivity.
• Ensuring proper housekeeping and workplace safety.
• Participating in investigations of deviations, non-conformances, and corrective actions.
• Supporting continuous improvement initiatives.

Qualifications and Experience

• Bachelor’s Degree or Diploma in Pharmaceutical Manufacturing, Pharmaceutical Sciences, Chemical Engineering, Industrial Production, or a related field.
• Minimum 5 years of relevant experience in a manufacturing industry.
• Demonstrated experience supervising production teams.
• Experience in pharmaceutical manufacturing will be a significant advantage.
• Knowledge of GMP, production documentation, quality systems, and occupational safety.
• Strong leadership and people-management skills.
• Ability to work under pressure and meet production targets.