Complete literature search including Patents, Journals, Internet and Encyclopaedias.
Pre-formulation studies and selection of excipients and process.
Pharmacokinetic Calculation to set up Dissolution Profile and use of IVIVC as a tool for formulation development.
To plan, organize and conduct Pharma research experiments to develop controlled release, sustained release, and immediate release oral solid, by using QBD principles and structured trial approach like DOE.
Involved in Fabrication of the developmental, Analytical Technology transfer, validation, scale up, Exhibit and Validation/commercial batches.
Preparation & Review of the documents like Master formula card, Manufacturing instruction, Stability protocol, Investigation protocol, Technology transfer dossier, Development report, Investigation report, scale up protocol, scale up report, test batch monitoring report.
Co-ordination with Analytical development Lab, Production, Purchase dept and QA/QC dept.
Query response to CQA points.
Higher education (pharmacy, chemistry).
Experience in formulation minimum 5 years.
Knowledge of technology and pharmaceutical formulation for solid dosage forms.
Experience in working with English documentation (translation, communication, written / verbal documentation).
PC operation (Word, Excel, Internet, email communication).
Ability to analyze and attention to detail.
Relative skills for finding solutions of common interest in departments and working groups.
Simultaneous and different approach to study subjects.
Initiative and new survey on the subject.
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