Key Responsibilities
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Execute and support in‑vitro studies, analytical activities, including NG tube and G‑tube studies, as per guidance and protocols.
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Ensure adherence to GLP and GDP requirements, including proper documentation, data integrity, and laboratory practices.
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Participate in analytical investigations, deviations, and CAPA activities.
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Maintain analytical instruments, including calibration and coordination with service teams as required.
Qualification & Experience
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B.Pharm, Master’s or Bachelor’s degree in Sciences,
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Experience with in‑vitro studies, including NG/G tube studies.
Key Skills & Competencies
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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
