- Perform physical testing and chemical analysis of different pharmaceutical dosage forms.
- Participate in investigation of any OOS case or NCR.
- Prepare and write the relevant quality control documents as specifications, analytical monographs, sampling processes and technical instructions.
- Implementation of good documentation practices (GDP) and good laboratory practices (GLP) in Qc labs.
- Handling & control of lab equipment during lab activities.
- Calibration of all analytical instruments in Quality Control Lab.
- Recording the activities in the operation and instrument logbooks.
- Participating in APR analysis by trending QC data.
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Bachelor of Science, or pharmacy.1 – 3 yearsGood manners.Work under pressure.Problem solving & Logic thinking.An Organized person.Teamwork.Has ability to improve & is able to learn.Good Communication skills.Basic Quality tools.Soft Skills (Time Management, Team Building)