India Job Openings
Ferring Pharmaceuticals, Inc.
Research Fellow - CMC (Analytical)
Hyderābād
FULL TIME
September 6, 2024
Location: Hyderabad
Duration: 12 months
Reports to: Associate Director - CMC (Analytical)
Department: CMC (Analytical)
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Assist in developing and validating analytical methods such as HPLC, GC, FTIR, NMR, UV-Vis, and dissolution testing.
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Support the optimization of analytical procedures to ensure precision, accuracy, and robustness.
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Conduct sample preparation, including dissolution, dilution, extraction, and filtration for testing.
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Perform routine and non-routine analyses of pharmaceutical samples, including APIs, excipients, and finished dosage forms.
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Ensure the accuracy of data collection, processing, and reporting.
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Document experimental procedures, observations, and results according to Good Laboratory Practices (GLP).
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Maintain detailed records in laboratory notebooks and prepare reports for review by senior scientists.
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Follow company protocols and regulatory guidelines (FDA, ICH, USP, etc.) to ensure compliance.
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Assist in interpreting analytical data and troubleshooting analytical methods.
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Present findings and provide recommendations during team meetings.
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Prepare technical reports, Standard Operating Procedures (SOPs), and analytical test methods.
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Ensure proper use, maintenance, and calibration of laboratory equipment.
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Adhere to all safety protocols, including the handling and disposal of chemicals and hazardous materials.
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Maintain a clean and organized laboratory environment.
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Work closely with other departments, such as formulation development, regulatory affairs, and quality assurance, to support drug development programs.
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Participate in project discussions and contribute to problem-solving initiatives.
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Completed/ awaiting final result - master’s in chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related field from a reputed university.
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Knowledge of analytical techniques such as HPLC, GC, and spectroscopy is preferred.
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Familiarity with regulatory guidelines (FDA, ICH) is a plus.
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Strong analytical, problem-solving, and organizational skills.
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Ability to work independently and in a team environment.
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Proficient in MS Office Suite (Word, Excel, Power Point).
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Excellent verbal and written communication skills.
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Gain practical, hands-on experience in a pharmaceutical R&D environment.
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Learn how to develop and validate analytical methods following regulatory guidelines.
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Understand the drug development process from an analytical perspective.
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Collaborate with multidisciplinary teams and gain exposure to cross-functional areas in drug development.
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