Summary
Date Posted: Sunday, January 19 2025, Base Salary: Not Disclosed

JOB DETAILS:
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.
1. To adhere to procedures on cGMP and GLP and relevant ISO procedures that guide all quality control processes.
2. Conduct quality control tests on water, bulk, raw materials stability samples and finished products.
3. Document and prepare reports for all Quality control activities performed online; calibrate and Maintain laboratory equipment as per the plan
4. Interpret all documents in QC process, revise and prepare SOPs and COAs as required in the process
5. Work effectively with other analysts and team leaders to achieve shared goals and meet timelines for batch processing and filling processes.
6. Participate in OOS, OOT investigation, deviation handling, change control, CAPA closure, and quality risk management for continuous improvement.
7. Participate in training, knowledge sharing, and transfer activities for efficiency and competency.
8. Sampling of RM, FP, preparation of reagent & standardization of reagent as per production plan requirements.
9. Calibration of new glassware.
10. Working standard preparation.
11. Handling & maintaining Reference standard as per reference standard SOPs, preparation of working standard.
12. 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
13. Perform method validation & verification for the new method and establish specifications.
14. Proper use and handling of chemicals and consumables
15. Perform online reporting & keep records.
16. Timely and proper Communication with staff at all levels while making critical escalation on time
17. Use provided personal protective gear appropriately.
18. 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

COMPETENCIES
1. Excellent report writing skills, analytical skills, communication skills, and interpersonal skills.
2. Computer skills, able to learn and adapt to change.
3. Innovative / creative skills and problem solving

MINIMUM QUALIFICATIONS / REQUIREMENTS
1. BSc Chemistry or equivalent Degree
2. Experience in pharmaceutical/healthcare industry is an advantage

Job Experience: No Requirements

Work Hours: 8

Experience in Months:

Level of Education: Bachelor Degree

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