Only 24h Left: Research Fellow

1 week ago

Hyderabad, Telangana, India Ferring Full time

Position Research Fellow -CMC Analytical Location Hyderabad Duration 12 months Reports to Associate Director - CMC Analytical Department CMC Analytical Role Overview The Analytical Research Development Intern will assist in the development validation and optimization of analytical methods used for the analysis of pharmaceutical products raw materials and intermediates The intern will gain hands-on experience with modern analytical techniques data interpretation and reporting contributing to the success of drug development projects Key Responsibilities Method Development Validation Assist in developing and validating analytical methods such as HPLC GC FTIR NMR UV-Vis and dissolution testing Support the optimization of analytical procedures to ensure precision accuracy and robustness Sample Preparation Analysis Conduct sample preparation including dissolution dilution extraction and filtration for testing Perform routine and non-routine analyses of pharmaceutical samples including APIs excipients and finished dosage forms Ensure the accuracy of data collection processing and reporting Documentation Compliance Document experimental procedures observations and results according to Good Laboratory Practices GLP Maintain detailed records in laboratory notebooks and prepare reports for review by senior scientists Follow company protocols and regulatory guidelines FDA ICH USP etc to ensure compliance Data Interpretation Reporting Assist in interpreting analytical data and troubleshooting analytical methods Present findings and provide recommendations during team meetings Prepare technical reports Standard Operating Procedures SOPs and analytical test methods Lab Maintenance Safety Ensure proper use maintenance and calibration of laboratory equipment Adhere to all safety protocols including the handling and disposal of chemicals and hazardous materials Maintain a clean and organized laboratory environment Cross-Functional Collaboration Work closely with other departments such as formulation development regulatory affairs and quality assurance to support drug development programs Participate in project discussions and contribute to problem-solving initiatives Qualifications Completed awaiting final result - masters in chemistry Pharmaceutical Sciences Chemical Engineering or a related field from a reputed university Knowledge of analytical techniques such as HPLC GC and spectroscopy is preferred Familiarity with regulatory guidelines FDA ICH is a plus Strong analytical problem-solving and organizational skills Ability to work independently and in a team environment Proficient in MS Office Suite Word Excel PowerPoint Excellent verbal and written communication skills Opportunities Learning Outcomes Gain practical hands-on experience in a pharmaceutical R D environment Learn how to develop and validate analytical methods following regulatory guidelines Understand the drug development process from an analytical perspective Collaborate with multidisciplinary teams and gain exposure to cross-functional areas in drug development Location Ferring India FHPDC R D

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