Formulation Scientist

Vizen Life Sciences Pvt Ltd; Hyderabad; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Vizen Life Sciences Pvt Ltd in Hyderabad seeks a Pharmacologist for end-to-end formulation development of OSD/Derma products. You will lead development, execution, filing and support for regulatory approvals, and collaborate across QA, Regulatory, Supply Chain and external partners.

The role covers process feasibility, equipment selection, scale-up, technology transfer, batch documentation, and on-site/remote technical support to ensure successful manufacturing.

Qualifications

• Educational qualification: Masters in Pharmaceutical
• Minimum work experience: 3–6 years in pharma industry (OSD/Derma products)

Responsibilities

• Responsible for end-to-end Formulation development including development, execution, filing and approval.
• Assess process feasibility to enable effective product and process knowledge transfer.
• Support selection of suitable manufacturing equipment and establish batch sizes based on plant capabilities.
• Prepare and review master manufacturing records, batch documents, technology transfer packages, development reports, and regulatory filing documentation.
• Execute and support scale-up, exhibit, validation, submission, and commercial batches.
• Ensure availability of equipment, materials, tooling, and supporting resources at the receiving manufacturing site.
• Provide on-site and remote technical support during technology transfer, validation, and commercial manufacturing.
• Collaborate with Manufacturing, Quality Assurance, Analytical Development, Regulatory Affairs, Supply Chain, and external partners to ensure successful project execution.
• Prepare investigation reports, technical assessments, and scientific justifications based on laboratory and manufacturing observations.
• Support manufacturing and Quality teams in implementing process improvements and corrective actions.

Education

Masters in Pharmaceutical

Job description

Responsibilities

• Responsible for end-to-end Formulation development including development, execution, filing and approval.
• Assess process feasibility to enable effective product and process knowledge transfer.
• Support selection of suitable manufacturing equipment and establish batch sizes based on plant capabilities.
• Prepare and review master manufacturing records, batch documents, technology transfer packages, development reports, and regulatory filing documentation.
• Execute and support scale-up, exhibit, validation, submission, and commercial batches.
• Ensure availability of equipment, materials, tooling, and supporting resources at the receiving manufacturing site.
• Provide on-site and remote technical support during technology transfer, validation, and commercial manufacturing.
• Collaborate with Manufacturing, Quality Assurance, Analytical Development, Regulatory Affairs, Supply Chain, and external partners to ensure successful project execution.
• Prepare investigation reports, technical assessments, and scientific justifications based on laboratory and manufacturing observations.
• Support manufacturing and Quality teams in implementing process improvements and corrective actions.

Qualification & Experience

• Educational qualification: Masters in Pharmaceutical
• Minimum work experience: 3 to 6 years of experience in pharmaceutical company in OSD/ Derma products.