Analyst, Qc
6 months ago
**Job Summary**:
Performing analysis and reporting of samples and may be assigned to any section such as raw material, finished product, validation, or stability, performs equipment calibration, documentation review, and confirmatory analysis within investigations, and participates in internal quality systems including training. This must be achieved through efficiency both in time and material resources, while ensuring compliance with GLP, company procedures, EH & S regulations as well as Pharmacopoeia standards.
**Job description**:
- Performs a variety of routine and basic tests in support of routine testing for stability batches, production of intermediate samples, finished products, Raw Materials, and process/cleaning validation samples to ensure that materials comply with the standards as per the approved Hikma Testing Method.
- Responsible for the proper implementation of 5S in the lab.
- Properly disposing of all contaminants and different hazardous and bio-hazardous materials.
- Preparation of chemical reagents and other required volumetric solutions.
- Reporting and documenting any incidents, out-of-specifications, and out-of-trend results according to the predetermined procedures.
- Possess good awareness of basic GMP & GDP requirements.
**Qualification**:
- BSC of Pharmacy or Science
- Minimum years of experience 1:3 years in QC.
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