Rubicon Research is a specialty pharmaceutical company focused on developing high quality products using innovative technologies for the global market. We are committed to designing effective value-added formulations that enrich lives around the world.
Vacancy details:
- Position: Formulation Development
- Qualification: B.Pharma, M.Pharma
- Experienced:2 – 4 years
- Salary: Not Disclosed
Job Description: -Greetings from Rubicon Research Pvt Ltd..!!
Important Details:
- Location: Thane,Maharashtra
- Post of date:27/12/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Job description
Responsible for the development of new products and optimization of existing formulas; product lines including traditional solid dosage products (tablets, capsules) and other delivery forms (e.g. liquids, powders).
- Responsible for formulation and process development of oral dosage forms, including oral solid and liquid formulations. Troubleshoot and problem-solve unresolved or new formula issues.
- Design and execute formulation trials and evaluate stability data to finalize formulation composition.
- Develop robust manufacturing processes for R&D formulations so that the technical transfer is successful for large scale batches.
- Responsible for all formulation/ process related CMC documents which will be part of regulatory filings.
- Write/review master formulas, manufacturing procedures, SOPs, stability protocols/reports, process validation protocols/reports, Product Development Reports, QOS, QbR etc.
- Support the manufacturing of exhibit/submission batches per regulatory requirements.
- Support technology transfer for manufacturing processes from laboratory scale to production scale.
- Works with Analytical Method 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 cGLPs.
- Provide recommendations for continuous improvements in practices and systems to improve performance and enhance efficiency and quality.
Qualifications & Pre-Requisites
- Masters Degree in Pharmaceutical sciences educational background with 1-3 years of experience in related field.
- Knowledge of regulatory guidances
- Exposure of pellet projects and liquid oral projects will be an added advantage for the role.
Concern Person
Pranali
HR Department
