Officer
3 weeks ago
**Minimum experience required in this position**:
**2+ years**:
**Description**:
**Roles & Responsibilities:
- **
- Working on Analytical Method Development of dosage forms like Oral Solids (Tablet & Capsules)&ndash IR tablets, Sustained release tablets, extended release tablets, Bilayer tablets, Capsule etc. & External preparations like Gels, Pastes, Creams, Ointments etc. under guidance of Team lead to find optimal Analytical method.
- Performing analysis of In-process samples & finished products samples of trial batches of F&D and finalised formulation stability study sample analysis.
- Performing Dissolution profile, pH & Solubility Study, Stability study of trial product and raw materials in wet lab & instrument lab.
- Properly documenting activities of the project under investigation under guidance of Team Lead.
- Preparing AMV and AMT protocols and reports as per regulatory and customer requirements under guidance of team lead.
- After finalization of method, Executing Analytical Method Validation as per guidance of Team lead.
- In case of absence of samples from F&D, performing QC routine analysis of RM, In-process & finished products.
- Performing analysis for Cleaning Method validation.
- Following QC SOP&rsquos, Good Laboratory Practices & Safety norms while working in Lab.
- Performing working instrument calibration as and when required.
**Highest Qualification:
- **
M.Pharm / M.Sc
**Location:
- **
Akola
-
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