Job Overview
-
Date PostedAugust 15, 2023
-
Location (State / UT)
-
Expiration dateAugust 14, 2024
-
Experience1 Year, 4 Years
-
GenderAny
-
Desired QualificationMaster’s Degree, Doctorate Degree
Job Description
- Assist in the development and optimization of Parenteral pharmaceutical formulations., Conduct literature research, gather data, and assist in designing experiments to support formulation development activities.
- Participate in the planning, design, and execution of formulation experiments. Prepare formulations, perform laboratory-scale tests, and analyze results to evaluate factors such as stability, solubility, compatibility, and bioavailability.
- Conduct routine analysis of formulation samples using various analytical techniques, such as HPLC, spectroscopy, particle size analysis, and dissolution testing. Assist in method development and validation activities to support formulation characterization and quality control.
- Collect and analyze experimental data, interpret results, and generate reports summarizing findings. Collaborate with senior scientists to draw conclusions and make recommendations for further formulation development or process optimization.
- Maintain accurate and detailed records of experimental procedures, protocols, results, and observations. Prepare technical reports, presentations, and documentation required for regulatory submissions and internal reviews.
Required Candidate profile
- M.Pharm or Ph.D. with 1-3 years experience. GATE/GPAT qualified