Dr. Reddys Lab

Prepare, review, and approve technical protocols, reports, and product impact assessments related to product lifecycle management.

The objective is to produce products within defined volumes and timelines while maintaining compliance with quality standards, GMP, and other regulatory and statutory requirements, as per the schedule.

Masters in pharma / Biotechnology / Chemistry at Dr. Reddys Lab. Seeking a dynamic and experienced Specialist in Process Development in the pharmaceutical development process, responsible for strategy evaluations, process design, optimization

A Bachelors degree in Pharmacy, Pharmaceutical Sciences, or a related field; advanced degree in Pharmaceutical Sciences or Regulatory Affairs is advantageous

A Graduation or Post Graduation in Science, including Pharma and Technology. Basic understanding of relevant techniques, including cell-based and ligand binding assays. Familiarity with fundamental biotechnology industry practices.

Your responsibilities include authoring process validation protocols and reports, conducting risk assessments, utilizing tools like Continued Process Verification (CPV), PAT Tools, and statistical analysis tools

Diploma/ B Tech, B.sc, MSc, B.Pharm, BTech or Masters in Biotechnology / Microbiology /Biochemistry

Implement and maintain quality control procedures within the QMS framework. Conduct thorough inspections and tests on products and materials at various stages of production

You will be responsible for preparation, review and submission of Dossier in ANZ and Emerging Markets as per the applicable regulatory guidance in Emerging Markets.