October 2025

The Central Drugs Standard Control Organization (CDSCO) has issued a directive to all State and Union Territory Drug Controllers, stressing the need for strict compliance with the Drugs Rules, 1945, in testing raw materials and finished pharmaceutical formulations.

Professionals having proven competency and success in conducting Quality Assurance and / or managing studies under GLP (Good Laboratory Practice environment, with at least 10 years of post- qualification experience, and should possess M.Sc./ M.V.Sc. / M.Pharm / M. Tech qualification.

Diploma in Pharmacy OR Bachelor Degree in Pharmacy (B. Pharm) from a recognized institution and registered as Pharmacist under the Pharmacy act 1948

M.Sc. degree in Zoology / Biochemistry / Biotechnology / Life Science with first class in graduation and post-graduation. 

Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. PG Diploma in Clinical Research is mandatory with one year experience is desirable.

Post-Graduate degree in any branch of Life Sciences, including the integrated PG degree, from the recognized university.

Ph.D. holder full-time Ph.D. project shall be related to Clinical Embryology or assisted reproductive technology or fertility from a recognised university with an additional one year of human ART laboratory experience.

Keep pace with and align with the market developments. Needs to be aware of market dynamics, fluctuations, innovations etc. Understands scientifically how various product are placed in relation to competitor products and devise appropriate strategies to deal with them

Alkem Laboratories Limited established in 1973, is amongst the top five leading Indian Pharmaceutical Companies with global operations.