Key Responsibilities
Execute and support in‑vitro studies, analytical activities, including NG tube and G‑tube studies, as per guidance and protocols.
Ensure adherence to GLP and GDP requirements, including proper documentation, data integrity, and laboratory practices.
Participate in analytical investigations, deviations, and CAPA activities.
Maintain analytical instruments, including calibration and coordination with service teams as required.
Qualification & Experience
B.Pharm, Master’s or Bachelor’s degree in Sciences,
Experience with in‑vitro studies, including NG/G tube studies.
Key Skills & Competencies
Good understanding of regulatory expectations and data integrity principles
Attention to detail and strong documentation skills
Effective communication and teamwork abilities
Ability to manage multiple activities and meet timelines
