Key Responsibilities:

• Responsible for the development of new products and optimization ofexisting formulas; product lines including solid dosage products (tablets,capsules) and other delivery forms (eg, liquids, powders) for regulated marketslike US, Europe and ROW.
• Responsible for formulation and process development of oral dosageforms, including oral solid and liquid formulations. Troubleshooting andproblem-solving of unresolved or new formula issues.
• Design and execute formulation trials and evaluate stability data tofinalize formulation composition.
• Develop manufacturing processes for R&D formulations so that thetechnical transfer is successful for large-scale batches.
• Write/review master formulas, manufacturing procedures, SOPs, stabilityprotocols/reports, process validation protocols/reports, Product DevelopmentReports, QOS, etc.
• Works with Analytical Method Development, Regulatory Affairs, QualityControl, Quality Assurance, Inventory Control, etc. to expedite the developmentand approval of new products by the FDA.
• Candidate should have hands-on/practical experience in development,technology transfer, and ANDA submissions for solid/ liquid oral dosage forms(solutions, suspensions, tablets, capsules) for regulated and semi-regulatedmarkets like the US, Europe, and ROW.
  

Required Educational Qualification and Relevant Experience:

• Minimum Master's Degree in Pharmaceutical Sciences with 1 Year relevant experience.