Scientist - Formulation Development(Oral Solids)

Dear All,

We are seeking a highly motivated and talented Formulation R&D Scientists to join our innovative team. The ideal candidate will have a strong foundation in formulation development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements.

Location: Hyderabad(Dulapally)

Required Experience: 6-8 Years

Job Responsibilities:

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 equipments/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 BMR, process evaluation plan, exhibit batch protocols, stability protocol, Dissolution profiling report, Assessment report, Tablet sub division study summary report and all documents related to Formulation development.

12. To drive all concerned documents from formulation development to exhibit batches and then to commercialization through document management system.

13. Coordinate to prepare the specifications for raw materials, in-process and finished product.

14. Preparation of product development reports (PDR)

15. Preparation of summary reports for exhibit and process evaluation batches.

16. Initiation of Change controls.

17. Initiation of document/ mandatory revision/withdrawal control form.

18. Initiation of departmental incidents.

19. Conducting departmental trainings.

20. Calibration of instrument/equipment pertaining to the department.

21. Preparation and processing of department SOPs/Guidelines/Operating instructions.

22. Preparation of summary reports for exhibit and process evaluation batches

Note: Interested candidates can share their resumes to [email removed] and Immediate joiners are more preferable