Job Title: Quality Control Analyst – Chemistry (Fresher Job Opportunities)
Organisation: Abacus Parenteral Drugs Limited (APDL)
Duty Station: Mukono, Uganda
Reporting to: QC Team Leader
About Organisation:
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.
Job Summary: 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.
Key Duties and Responsibilities:
- To adhere to procedures on cGMP and GLP and relevant ISO procedures that guide all quality control processes.
- Conduct quality control tests on water, bulk, raw materials stability samples and finished products.
- Document and prepare reports for all Quality control activities performed online; calibrate and Maintain laboratory equipment as per the plan
- Interpret all documents in QC process, 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 as per production plan requirements.
- Calibration of new glassware.
- Working standard preparation.
- Handling & maintaining Reference standard 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 specification
- Perform method validation & verification for the new method and establish specifications.
- Proper use and handling of chemicals and consumables
- Perform online reporting & keep records.
- Timely and proper Communication with staff at all levels while making critical escalation on time
- Use provided personal protective gear appropriately.
- Proper communication and handling and investigation of all incidences, near misses and accidents
Qualifications, Skills and Experience:
- BSc Chemistry or equivalent Degree
- Experience in pharmaceutical/healthcare industry is an advantage
Competencies
- Excellent report writing skills, analytical skills, communication skills, and interpersonal skills.
- Computer skills, able to learn and adapt to change.
- Innovative / creative skills and problem solving
How to Apply:
Kindly submit your updated CV and academic credentials to [email protected]
Deadline: 24th. January 2025 by 5 Pm
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Level of Education: Bachelor Degree
Work Hours: 8
Experience in Months: No requirements