Aizant Drug Research Solutions Pvt. Ltd – Walk-In Interviews for FR&D / AR&D on 17th – 18th Feb’ 2023

Walk-In-Interview for Jr. Scientist / Scientist – Formulation & Analytical Development (OSD)

Formulation Research & Development (OSD):

1. Plan and execute Pre-formulation and formulation activities and ensure the timely execution of project-related tasks in coordination with team members.
2. Actively participate in the literature search and preparation of formulation development strategy.
3. Coordinate with the QA department for getting forms and logbooks.
4. Follow good laboratory practices, and good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments.
5. Coordination and participation in internal department audits/sponsor or client audits.
6. Coordination with the purchase/sourcing department for procurement of materials.
7. Participation in the qualification of equipment/instrument pertaining to the department.
8. Compilation, interpretation, and review of analytical results and stability data.
9. Submission of documents and coordination with liaison personnel for procuring required licenses for carrying out the development work.
10. To initiate the project and allot the product identification codes.
11. Preparation of Master formula card (MFC), scale-up protocol, process evaluation plan, exhibit batch protocols, and stability protocol.

Analytical Research & Development (OSD):

1. To ensure error-free and online documentation.
2. Ensure only calibrated instruments/equipment are used for analysis.
3. Coordinate with supervisor in developing the methods for dissolution, assay by UV/HPLC, RS by HPLC, and Residual solvents by GC.
4. To perform analysis of development samples for Dissolution, Assay by UV/HPLC, RS by HPLC
   and Residual solvents by GC as per the test method.
5. Perform validation of test procedures like Dissolution, Assay, Related substances, Residue
   and Chiral purity etc.,
6. Ensure the instruments/equipment are cleaned after completing the analysis.
7. Daily monitoring of temperature in refrigerator and labs.
8. Receipt and storage of samples/standards.
9. Labeling of standards, chemicals, and reagents.
10. Receipt of log books and SOPs from QA.
11. To ensure GLP compliance in the laboratory.

WALK-IN-INTERVIEW DETAILS: