QC Analyst

Full Job Description

Job Description & Requirements

1. Samples and/or finished products from manufacturing, to ensure quality standards and compliance with established specifications.
2. Preparation of reagents, diluents, and dissolution media as per STP.
3. Perform various qualitative tests or qualitative assays on samples using modern and automated instrumentation.
4. Utilize electronic laboratory information systems such as LIMS for acquisition and processing of analytical data.
5. Assist in maintenance and calibration of test instruments per specifications.
6. Responsible for the accurate, timely, and compliant execution of assigned projects, analytical testing, and related documentation.
7. Knowledge of analytical chemistry, chromatography (HPLC/GC), and drug dissolution testing.
8. Familiar with LIMS and reporting of any observed results that do not meet the requirement [OOS/OOT/Deviation] for further investigation.
9. Destruction of expired finished products/raw material samples as per SOP and recording the same in the register.
10. Ensure real-time documentation.
11. Maintain data integrity and appropriate traceability.
12. Thorough knowledge and understanding of BP, USP, cGMP, and FDA guidelines.
13. Maintain a clean and safe work environment and follow safety procedures and policies.
14. Create and maintain lab record documentation (notebooks and computer-based) per GMPs.

EDUCATION & EXPERIENCE:

1. Degree/Diploma in a science-related discipline.
2. Minimum 2 years of experience in a pharmaceutical environment.

Candidates are encouraged to apply for this position via email to lincy.lim@pharmagend.com with the following information in the resume:

1. Work experiences and job responsibilities
2. Current and expected salary
3. Reason for leaving
4. Date of availability
5. Education background
6. Only shortlisted applicants will be notified.