Formulation And Development Officer

Qualigens Pharma; Khopoli; On-site; INR 600,000 - 900,000; Full time

Job summary

Qualigens Pharma in Maharashtra, Khopoli invites a formulation development scientist to contribute to tablet and capsule development, scale-up planning, and documentation reports. The role covers literature review, proof of concept, and process parameter development with emphasis on regulatory-ready practices.

You will generate Master Formula Records and Product Development Reports, support stability studies, and troubleshoot tech transfers to new products, ensuring laboratory compliance and

Qualifications

• Formulation development for tablets and capsules.
• Experience with scale-up of batches for production.
• Preparation of Master Formula Record (MFR) and Product Development Report (PDR).
• Technical troubleshooting of transferred products.

Responsibilities

• Literature review, carrying out proof of concept, feasibility & formulation trials.
• Performing in-process tests as part of formulation trials.
• Performing pre-formulation studies including drug-excipient compatibility studies.
• Sourcing raw & packaging materials, tooling as per regulated market requirements.
• Planning & executing the scale-up batches and production level
• Determination & developing manufacturing process parameters.
• Recording & completing raw data in lab note books, preparing Master Formula Record, Product Development Reports & supporting documents.
• Packaging & preparing products for R&D stability studies, subjecting the samples for stability studies, monitoring, compiling the results and preparing the stability report.
• Maintaining the lab equipment & instruments in good condition & following Good Laboratories Practices.
• Working towards new product & process development ideas.

Skills

Formulation development

Scale-Up batches

Master Formula Record

Product Development Report

Troubleshooting

Job description

Role & responsibilities

• Literature review, carrying out proof of concept, feasibility & formulation trials.
• Performing in-process tests as part of formulation trials.
• Performing pre-formulation studies including drug-excipient compatibility studies.
• Sourcing raw & packaging materials, tooling as per regulated market requirements.
• Planning & executing the scale-up batches and production level
• Determination & developing manufacturing process parameters.
• Recording & completing raw data in lab note books, preparing Master Formula Record, Product Development Reports & supporting documents.
• Packaging & preparing products for R&D stability studies, subjecting the samples for stability studies, monitoring, compiling the results and preparing the stability report.
• Maintaining the lab equipment & instruments in good condition & following Good Laboratories Practices.
• Working towards new product & process development ideas.

Preferred candidate profile

Should be comfortable in Formulation development of tablets & capsules.

Should be comfortable in Planning and Execution of Scale -Up Batches

Should be comfortable in preparing Master Formula Record & Product Development Report.

Should be comfortable in Technical Troubleshooting of tech transferred products.