Experience: 5 - 8 yrs
contact@genpharma.ma
- Develop analytical methods, conduct validations of these methods and analytical method tech transfer.
Prepare Method Development and Method Validation protocols and reports.
You should have thorough understanding of instruments like HPLC with various detection systems, GC, various Dissolution models, UV, IR.
Conduct forced degradation study & identification of unknown impurities.
Analysis of pre-formulation batches.
Analytical trouble shooting, independent problem solving ability.
Carry out stability study at each stage of formulations development.
Maintain lab equipments as per GMP/GLP.
Actively participate in regulatory inspections.
Investigate abnormal results and discuss them with group leaders.
Visualize the developmental needs of the formulation.
Understand the safety and environmental aspect.
Analyze the formulation strategy, efficiency, working relations and cross-functional coordination.
Calibrate the instruments according to the master calibration schedule and follow GLP and follow SOPs and STP.
Do literature search and study.
- Qualification requirement: Master of Science (MSc) / B. Pharm / M.Pharm
- Yaseen Momin
contact@genpharma.ma
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