SKant Hiring Microbiology Analyst & Jr Documentation Officer

MSc Microbiology QC Jobs at SKant East Africa | Namanve

SKant East Africa hiring Microbiology Analyst (OSD QC) & Jr Documentation Officer at Namanve. MSc Microbiology, Science graduates, 2–5 yrs experience.

SKant East Africa Ltd., a long-established pharmaceutical organization with a legacy of serving healthcare since 1932, is inviting applications from qualified and experienced professionals for Quality Control and Documentation roles at its modern manufacturing facility located in Namanve Industrial Park. These opportunities are ideal for candidates seeking stable pharmaceutical careers within a regulated GMP environment that values quality, compliance, and continuous improvement.

Company Overview

SKant East Africa Ltd. operates as part of a diversified healthcare group with decades of experience in pharmaceutical manufacturing and quality-driven operations. The organization follows globally accepted GMP standards and emphasizes data integrity, patient safety, and regulatory compliance across all departments. With consistent investments in infrastructure, systems, and people, SKant East Africa continues to strengthen its position as a trusted pharmaceutical manufacturer in the region.

The Namanve Industrial Park facility is equipped with advanced laboratories, controlled manufacturing areas, and structured quality systems that support solid oral dosage form production and documentation-driven operations.

Job Role & Responsibilities – Microbiology Analyst (OSD QC)

The Microbiology Analyst will be responsible for routine and advanced microbiological testing activities to ensure product safety, compliance, and quality across OSD manufacturing operations.

Key Responsibilities

• Perform environmental monitoring (EM) of classified areas, including air and surface monitoring.
• Conduct water testing, microbial limit tests (MLT), bioburden analysis, and finished product microbiological testing.
• Prepare, sterilize, and perform growth promotion testing (GPT) of microbiological media.
• Operate and maintain laboratory equipment such as LAFs, incubators, autoclaves, and air samplers.
• Record analytical results accurately in logbooks, worksheets, and reports following ALCOA+ data integrity principles.
• Prepare and revise SOPs, STPs, and microbiology-related documentation.
• Support OOS, OOT investigations, deviations, and CAPA implementation.
• Assist during internal audits, regulatory inspections, method validation, and method transfer activities.
• Ensure biosafety practices and proper waste disposal compliance at all times.

Job Role & Responsibilities – Junior Officer Documentation

The Junior Officer – Documentation role focuses on GMP documentation, production records, and quality system compliance across shop-floor operations.

Key Responsibilities

• Prepare, review, and maintain production SOPs and related GMP documents.
• Handle change control processes, deviations, incidents, and QRM documentation.
• Update production records, equipment lists, logs, and EPP plans.
• Maintain training records and coordinate GMP training programs for production teams.
• Review Batch Manufacturing Records (BMR) for accuracy and compliance.
• Report GMP non-compliance issues to the Production Head and support corrective actions.
• Ensure departmental cleanliness, discipline, and adherence to GMP standards.
• Participate in SQE meetings and promote a strong quality culture on the shop floor.

Eligibility / Qualifications

Microbiology Analyst – OSD QC

• Qualification: M.Sc. in Microbiology
• Experience: 3–5 years of experience as a QC Analyst in a pharmaceutical company
• Strong knowledge of GMP, aseptic practices, data integrity, and microbiological testing

Junior Officer – Documentation

• Qualification: Science Graduate
• Experience: 2–3 years of experience in pharmaceutical documentation or production quality systems
• Strong understanding of GMP, SOP documentation, quality systems, and data integrity

Location & Salary

• Work Location: Namanve Industrial Park
• Salary: Competitive and commensurate with experience (as per company standards)

Application Process

Interested candidates are requested to send their academic documents, updated CV, and a brief cover letter to:

Email: hr@skant.ug

Deadline to Apply: 2nd January 2026

Candidates are advised to apply early, as applications will be reviewed on a rolling basis.

Frequently Asked Questions (FAQs)

Who can apply for the Microbiology Analyst role?
Candidates with an MSc in Microbiology and 3–5 years of pharmaceutical QC experience are eligible.

Is prior pharmaceutical experience mandatory?
Yes. Experience in a GMP-regulated pharmaceutical environment is required for both roles.

Where is the job location?
Both positions are based at Namanve Industrial Park.

How do I apply?
Send your CV, academic documents, and cover letter to hr@skant.ug before 2nd January 2026.

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Company	SKant East Africa Ltd.
Vacancies	Microbiology Analyst – OSD QC, Junior Officer – Documentation
Required Education	MSc Microbiology, Science Graduate
Experience	2–5 Years