A Bachelors degree in Pharmacy, Pharmaceutical Sciences, or a related field; advanced degree in Pharmaceutical Sciences or Regulatory Affairs is advantageous
Perform literature search, laboratory trials for formulation development and process optimization studies of Oral solids and Liquids formulations. Stability data, characterization data generation complying to drug regulatory & quality requirements.
Interpret complex chromatographic data and ensure accurate documentation and reporting. Maintain and calibrate GC and GC-MS/MS instruments, ensuring compliance with regulatory standards.
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