Intern - CMC (Analytical)

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Posted:5 days ago| Platform: SimplyHired logo

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Job Type

Full Time

Job Description

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

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