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Ferring Therapeutics
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Intern - CMC (Formulation)

Intern - CMC (Formulation)

Ferring Therapeutics

1 - 6 years

0 Lacs

Hyderabad

Posted:1 day ago| Platform:

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Skills Required

Data analysis Pharmaceutics Intern Formulation Analytical Pharma CMC GLP Manager Quality Control Internship

Work Mode

Work from Office

Job Type

Internship

Job Description

Job Title: Intern CMC (Formulation)

Duration: 12 Months (1 year)
Location: Hyderabad
Department: CMC (Formulation)

Reporting To: Lead Scientist - CMC (Formulation)

Stipend: Paid

Qualifications:

Master s degree in Pharmaceutical Sciences (Pharmaceutics) or related discipline from a reputed institution.
Strong academic background in pharmaceutics
Basic knowledge of formulation principles and analytical techniques.
Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) is an advantage.
Proficient in MS Office (Word, Excel, PowerPoint) and scientific writing.
Excellent communication, organizational, and problem-solving skills.

Position Summary:

The Formulation R&D Intern will support the development of pharmaceutical dosage forms through hands-on laboratory work, data analysis, and documentation. This internship is designed to provide comprehensive exposure to formulation science, regulatory requirements, and industrial practices in a dynamic and collaborative environment.

Key Responsibilities:

Formulation Development:

Assist in the design and optimization of formulations for various dosage forms including tablets, capsules, suspensions, emulsions.
Conduct pre-formulation studies such as solubility, pH stability, hygroscopicity, and compatibility testing.
Participate in excipient selection and formulation trials based on physicochemical properties and target product profile.

Laboratory Work:

Prepare lab-scale and pilot-scale batches under supervision.
Operate and maintain laboratory equipment such as mixers, granulators, tablet presses, and dissolution testers.

Documentation & Compliance:

Maintain accurate and detailed laboratory notebooks and batch records.
Prepare technical reports and summaries of experimental findings.
Ensure compliance with Good Laboratory Practices (GLP)

Cross-Functional Collaboration:

Work closely with Analytical R&D, Quality Control, Regulatory Affairs.
Participate in project meetings and contribute to formulation strategy discussions

Location: Ferring India FHPDC R

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