Should know about injectable drug products and has minimum knowledge or experience in
Parenteral dosage forms.
Day to day execution of the experiments as per the plan and ensuring the requirements as per
the planning.
Open to learn about the dosage forms and the handling of formulation equipments like
Homogenizers Microfluidizers lyophilizer etc.
Co-ordination with cross functional teams (Analytical QA and PMO) and ensuring the smooth
execution of experiments.
Stability samples pull out and submission as per the protocol RLDs utilization RMs and PPMs
components inventory management.
Preparation of documents like stability protocols and reports analytical development studies
reports product development reports etc.
Implementation/ monitoring of laboratory GLP and safety practices.
SOP learning undersanding of GDP and GMP practices and execution without quality incidents
or error free experiments
Instrument maintenance log books Experiments writing in LNBs to be ensured
Any other responsibility assigned by the reporting manager.
Should know about injectable drug products and has minimum knowledge or experience in Parenteral dosage forms. Day to day execution of the experiments as per the plan and ensuring the requirements as per the planning. Open to learn about the dosage forms and the handling of formulation equip...
Should know about injectable drug products and has minimum knowledge or experience in
Parenteral dosage forms.
Day to day execution of the experiments as per the plan and ensuring the requirements as per
the planning.
Open to learn about the dosage forms and the handling of formulation equipments like
Homogenizers Microfluidizers lyophilizer etc.
Co-ordination with cross functional teams (Analytical QA and PMO) and ensuring the smooth
execution of experiments.
Stability samples pull out and submission as per the protocol RLDs utilization RMs and PPMs
components inventory management.
Preparation of documents like stability protocols and reports analytical development studies
reports product development reports etc.
Implementation/ monitoring of laboratory GLP and safety practices.
SOP learning undersanding of GDP and GMP practices and execution without quality incidents
or error free experiments
Instrument maintenance log books Experiments writing in LNBs to be ensured
Any other responsibility assigned by the reporting manager.
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