vacancies

Having exposure related Environment Monitoring in formulation, water analysis, various Microbiological test like sterility, BET, MLT etc. Having exposure related to regulatory plant and basic know of GLP GMP .Ready to work in rotational shift.

To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches.

Contribute to preparation including authoring where relevant and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and, or regional perspective.

The incumbent will be responsible for leading the overall Quality function for the organization. The Head –Quality will guide and lead members of the Quality Assurance and Quality Control teams to deliver as per the corporate goals, projects, plans and timelines.

Regulatory Affairs professionals with 5 to 8 years of experience in regulatory strategy, dossier review, and submission for the US, EU, and Brazil markets.

Oversee QC Lab Operations, Manage Chemical and Instrumental Analysis, and Ensue Compliance with Regulatory Standards.

B.Pharmacy or 10 plus 2 with Science and Diploma in Pharmacy. Preference will be given to the Ex-Servicemen.

Ph.D. in clinical sciences, life sciences, pharmacy, public health, healthcare, or other related disciplines with at least 2 years of work experience in Clinical Project Management and, or Clinical trial, Study monitoring

Only Indian citizens who are resident of Uttar Pradesh are eligible for Research Asst ships, Associate ships in the research projects funded by CST UP. The candidate must hold a degree of M.Sc. Ag M.Sc, M. Pharm, M.V.Sc, Bachelor of Engg, Technology B.E, B. Tech, or equivalent degree.