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Abacus Parenteral Drugs Limited (APDL) is a state of the art manufacturing facility that seamlessly integrates hi-tech engineering services into the building design. From the exterior view, the 36-acre APDL campus exudes careful planning, the interiors of the facility reveal thoughtful and spot on detailing. The facility is designed with materials and finishes that allow ample natural light thus conserving energy and still maintain high cleanliness standards and minimize maintenance. The entire facility is designed to meet the CGMP requirements.
Full-time
Quality Control Analysts-Chemistry (3) Job at Abacus Parenteral Drugs Limited (APDL)
Abacus Parenteral Drugs Limited (APDL)
Job Description
We’re Hiring | Join Our Growing Team
Abacus Parenteral Drugs Limited is looking for passionate, skilled, and motivated professionals to join our dynamic team across multiple departments.
We are currently recruiting for the following positions:
DESIGNATION: QC Analyst-Chemistry(03)
JOB IDENTIFICATION:
Department: Quality Control
Reporting to: QC Team Leader
POSITION PURPOSE:
To ensure effective and timely testing of all samples in accordance with requirements and in line with fast and changing quality procedures and principles, prioritization of testing, management of resources, and effective communication at all levels are necessary.
Duties, Roles and Responsibilities
JOB ROLES AND EXPECTATIONS:
Key Result Area
Key Roles / Duties
Quality
- To adhere to procedures on cGMP and GLP and relevant ISO procedures that guide all QC processes.
- Conduct quality control tests on water, bulk, raw material stability samples, and finished products.
- Document and prepare reports for all Q.C. activities performed online; calibrate and maintain laboratory equipment as per the plan.
Technical Work
- Interpret all documents in QC process and revise and prepare SOPs and COAs as required in the process
- Work effectively with other analysts and team leaders to achieve shared goals and meet timelines for batch processing and filling processes.
- Participate in OOS, OOT investigation, deviation handling, change control, CAPA closure, and quality risk management for continuous improvement.
- Participate in training, knowledge sharing, and transfer activities for efficiency and competency.
- Sampling of RM, FP, preparation of reagent & standardization of reagent per production plan requirements.
- Calibration of glassware of new glassware’s.
- Working standard preparation.
- Handling & maintaining reference standards as per reference standard SOPs, preparation of working standard.
- Perform analysis for intermediate sample, finished product sample, Raw material sample, stability sample, PPM & SPM as per work plan ensure it will meet with specifications.
- Perform method validation & verification for new method and establish specifications.
- Proper use and handling of chemicals and consumables
Reporting & Communication
- Perform online reporting & keep records.
- Timely and proper communication with staff at all levels while making critical escalation on time.
Safety
- Use provided personal protective gears appropriately.
- Proper communication and handling and investigation of all incidences, near misses and accidents
AUTHORITIES:
- Chemical analysis of all types of samples.
- Signing work reports.
- Request reports & logbooks.
- Release intermediate samples.
- Request for chemical & glassware.
Qualifications, Education and Competencies
See all details of the qualifications, competencies and education for this role under the "How to Apply" section below.
If you are ready to grow your career with one of East Africa’s leading pharmaceutical manufacturers, we encourage you to apply today.
Deadline: 20/05/2026
Please send your CV and academic credentials to apdlug.careers@abacuspharma.com before 5:00 PM on 20/05/2026.
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