This role is pivotal in managing activities pertaining to product lifecycle management, quality management and pharmacovigilance, including variations and renewals, SOP development, risk management, and trainings.
Candidates who have completed their courses and have their Provisional Certificate (mandatory), Degree Certificate/ All Semester Marksheets ONLY considered.
Maintain equipment logbooks, calibration records, and analytical test data sheets. Preparation and qualification of working standards, reference standards, and primary standards.
M.Sc / M.Tech in Nanotechnology / Biotechnology / Biochemistry / Biomedical Science / Microbiology with consistently good academic record and a minimum of 60% marks or an equivalent CGPA in the Masters degree.
Bachelors / Masters degree in Pharmaceutical Sciences, Chemistry, or related discipline. Strong knowledge of HPLC, GC, Dissolution, and other analytical techniques.
Hiring dynamic and self-motivated individuals to work in our Production Department, focusing on manufacturing pharmaceutical products in compliance with quality and safety standards.