Experience
- 1 to 5 years
Education
M.Pharm/B.Pharm from any reputed university with sound academic records.
Requirements
- 1 to 5 years
Additional Requirements
- Age At most 30 years
Practical knowledge of formulation development, stability studies and pharmaceutical product development.
Computer proficiency, including MS Office applications and professional email communication.
Responsibilities & Context
Conduct pre-formulation studies and develop, optimize and evaluate formulations for new and existing pharmaceutical products.
Perform laboratory, pilot and scale-up batches and support technology transfer to commercial production.
Conduct stability studies, evaluate results and prepare stability protocols, reports and related technical documents.
Investigate and resolve formulation, manufacturing, process and product stability-related issues.
Develop and validate analytical methods and prepare relevant technical documents for product evaluation and regulatory submission.
Prepare and maintain product development documents, including product specifications, master formula, BMR, BPR, validation protocols and reports.
Prepare product dossiers, recipes, annexures and supporting documents for DGDA registration, renewal and post-registration changes.
Coordinate with QA, QC, Production, Regulatory Affairs and other relevant departments to ensure successful product development and commercialization.
Ensure all product development activities comply with cGMP, applicable regulatory requirements and approved SOPs.
Job Other Benifits
Provident Fund, Gratuity, Festival Bonuses Health service benefits as per company policy