Formulation research & Development

Company Description Chemo India Formulation Pvt. Ltd, part of INSUD PHARMA, focuses on developing and manufacturing high-quality pharmaceutical formulations for diverse therapeutic areas. The organization is committed to innovation, regulatory compliance, and patient-centric solutions. As part of a global pharmaceutical group, the company offers exposure to international standards, advanced technologies, and cross-functional collaboration. Team members benefit from a professional environment that values integrity, safety, and continuous learning.
Role Description This is a full-time, on-site Formulation Research & Development role based in the Greater Hyderabad Area. The role involves designing and developing new formulations, optimizing existing products, and conducting pre-formulation and formulation studies in alignment with regulatory and quality requirements. Daily tasks include planning and executing laboratory experiments, documenting procedures and results, interpreting data, and collaborating with cross-functional teams such as QA, QC, and regulatory affairs. The position also requires preparing technical reports and development dossiers, supporting technology transfer to manufacturing, and contributing to process improvements and troubleshooting during scale-up.
Qualifications
Strong foundation in Research and Development (R&D) and applied Research within pharmaceutical formulations.
Proficient Analytical Skills for data interpretation, method evaluation, and problem-solving.
Solid Laboratory Skills, including handling formulation equipment, following SOPs, and maintaining safety and quality standards.
Effective Communication skills for clear documentation, reporting, and collaboration with internal and external stakeholders.
Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related discipline.
Knowledge of regulatory guidelines (e.g., cGMP, ICH) and familiarity with stability studies and validation processes.
Ability to work systematically, manage multiple projects, and meet timelines with attention to detail.
Previous experience in formulation development, scale-up, or technology transfer in the pharmaceutical industry is an advantage.

Work arrangement
No