Hiring for Rubicon Research Recruiting For Officer – Formulation Development ( R and D )

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..!!

ImportanDetails:

  • 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

[email protected]

HR Department

Leave a Comment