Qualification & Experience
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B.Pharm, M.Pharm, Master’s or Bachelor’s degree in Sciences,
- Experience with in‑vitro studies, including NG/G tube studies, is highly preferred.
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Hands‑on experience in analytical method development within the pharmaceutical or CRO/CMO environment.
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Strong working knowledge of in-vitro dissolution testing, HPLC, and related analytical techniques.
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Ensure adherence to GLP and GDP requirements, including proper documentation, data integrity, and laboratory practices.
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Experience in protocol and report preparation for development, validation and study.
Key Skills & Competencies
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Strong analytical and problem‑solving skills
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Good understanding of regulatory expectations and data integrity principles
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Attention to detail and strong documentation skills
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Effective communication and teamwork abilities
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Ability to manage multiple activities and meet timelines
