June 2026

M.Sc./ M.Tech (or equivalent) in Life Science or related areas. A score in any National level examination (CSIR/UGC/ICMR/DBT/ICAR) is preferable

Masters degree in Microbiology, Molecular Biology, Biotechnology, or a related field. Strong hands-on experience in microbial culture, DNA isolation, PCR, plasmid preparation, transformation, and NGS.

Candidate should have good experience in execution and review of qualification activities, environmental monitoring, clean room validation, and cross-functional coordination with Engineering, QA, and Production teams.

BDR Group of companies has grown steadily and become a house-hold name in the pharmaceutical Industry over the last 15 years, in both domestic and international arenas

Strong understanding of formulation analytical method development. Working knowledge of ICH guidelines, SAP. and documentation systems.

Workmen allocation and manpower management on shift basis. Supervision of secondary packing operations, especially bottle lines. Compliance with cGMP, safety, and hygiene requirements.

Exposure to OSD Manufacturing operations like Granulation, Pellet coating, Compression, Coating, Capsules, Primary Packing

Seeking a highly experienced Regulatory Affairs professional to manage regulatory activities for parenteral (injectable) products across the LATAM region. The role involves end-to-end regulatory lifecycle management, ensuring timely submissions, approvals, and compliance with regional regulatory requirements.

The ideal candidate must have hands-on experience in ophthalmic formulations, along with strong expertise in autoclave handling and batch manufacturing processes. Knowledge of GMP and quality compliance is essential.