Pharmacy

QA Specialist will serve as QA technical subject matter expert for CSV process, such as MES, KNEAT, DCS, including but not limited to GMP enterprise systems, manufacturing systems and computerized equipment, laboratory systems and computerized equipment and validation software tools.

To implement, manage and ensure the functions of GCP, GLP Quality Assurance program that will assure all BA, BE studies and clinical studies to withstand regulatory scrutiny.

Knowledge of the methods and procedures involved in the proper handling, dispensing and storing of pharmaceutical materials; Knowledge of basic labeling, measuring and weighing devices; Ability to take accurate arithmetical computations; Ability to understand and carry out oral and written instructions; Ability to keep accurate records; Ability to lift and move heavy objects.

Ph.D. in Science, Engineering, Technology, Veterinary Science, Pharmacy. Candidate must possess certificate, marksheet of basic knowledge of Computer from training institute or should have results with computer as a subject in degree or diploma curriculum from Government approved University or should have passed 10th or 12th examination with computer as a subject as prescribed by GAD in Government Resolution

Awareness of global regulatory reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting.

B.Pharm OR D.Pharm with working experience in Dispensary/ Pharmacy of the Hospital having minimum 200 beds. Registration with State Pharmacy Council

Development of Animal Feed Products from Eri Silkworm; Indian Institute of Technology Guwahati, the sixth member of the IIT fraternity, was established in 1994.

Graduate or Post Graduate in Science Life Sciences, Microbiology, Biotechnology, Pharmacy, BDS, BHMS, BAMS, MBBS etc. with post Graduate Degree or Diploma in Clinical Research.

Ensure preparation, review and submission of CTD sections in compliance with requirements of EMA, USFDA and other global markets. Timely update and preparation of dossier and documents as well as responses to the queries raised by regulatory agencies