Job Description
– Perform physical testing and chemical analysis of different pharmaceutical dosage forms.
– Prepare and standardizes volumetric solutions, reagents, dissolution media and buffers.
– Follows the controlled standard operating procedures and work instructions of finished product specifications and test methods during analysis process.
– Maintain the quality control approved control records related to the daily work.
– Issues and signs test certificates.
– Report and participate in investigation of any OOS case or NCR.
– Review, Check & follow up all results of bulk, semi-finished & finished product.
– Prepare and write the relevant quality control documents as specifications, analytical monographs, sampling processes and technical instructions.
– Training the analysts & Subordinates.
– Implementation of good documentation practices ( GDP ) and good laboratory practices (GLP) in Qc labs.
– Follow up and review subordinates.
– 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
– Aware and follow safety measures in the lab.
– Participating in APR analysis by trending QC data
Skills
o Work under pressure.
o Problem-solving & Logic thinking.
o An Organized person.
o Teamwork.
o Has ability to improve & is able to learn.
o Good Communication skills.
o Basic Quality tools.
Soft Skills (Time Management, Team Building).