Executive

2 days ago


New Delhi, India Rubicon Research Limited Full time

- Responsible for formulation and process development of Oncology and hormonal products of oral dosage forms (Oral solid and Oral liquid formulations). Troubleshooting and problem-solving of unresolved or new formula issues. - Design and execute formulation trials and evaluate stability data to finalize formulation composition. - Develop manufacturing processes for R&D formulations so that the technical transfer is successful for large scale batches. - Write/review master formulas, manufacturing procedures, SOPs, stability protocols/reports, process validation protocols/reports, Product Development Reports, QOS etc. - Support the manufacturing of exhibit/submission batches per regulatory requirements. - Support technology transfer for manufacturing processes from laboratory scale to production scale. - Guide to junior team members for routine activities. - Works with Analytical Development, Regulatory Affairs, Quality Control, Quality Assurance, Inventory Control, etc. to expedite the development and approval of new products by FDA. - Assure that all formulation and process development activities are documented in the notebook as per company procedures and cGMPs.Requirements:- Minimum Master’s Degree in Pharmaceutical sciences with 5+ years relevant experience. - Candidate should have hands on/practical experience in development, technology transfer and ANDA submissions for solid/ liquid oral dosage forms (solutions, suspensions, tablet, capsules) for regulated and semi-regulated markets like US, Europe and ROW. - Broad knowledge base of pharmaceutical sciences and processing in the Pharma industry



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