Research Fellow – CMC (Analytical)
Job Description:
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 – master’s 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
