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

Aizant Drug Research Solutions Pvt. Ltd is an integrated drug development solutions provider. Aizant was established by experienced pharmaceutical professionals with global exposure. We are a rapidly growing formulation CDMO and CRO with a diverse portfolio of capabilities partnering with health care companies specializing in new molecular entities (NME’s), generics (ANDA’s) and over the counter (OTC’s) products globally.

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 QA department for getting forms and logbooks.
4. Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments.
5. Coordination and participation of internal department audits / sponsor or client audits.
6. Coordination with purchase/sourcing department for procurement of materials.
7. Participation in 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, and exhibit batch protocols, stability protocol.

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Analytical Research & Development (OSD):

1. To ensure the error free and online documentation.
2. To ensure only calibrated instrument /equipments are used for analysis.
3. To 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 test method.
5. Perform validation of test procedures like Dissolution, Assay, Related substances, Residue
   and Chiral purity etc.,
6. To 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 the GLP compliance in laboratory.

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WALK-IN INTERVIEW DETAILS: