We at Encube Ethicals
Hiring for the Formulation Development Department.
Experience in Semisolid dosage forms is mandatory.
Qualification : M.Pharm
Experience : 5 – 7 years
Location : Dombivali (Palava)
Key Deliverables :
- Patent and Literature Search.
- Execute product development activities as per project requirements and timelines.
- Observe, analyse, and document key parameters during trial and stability batches.
- Maintain accurate and up-to-date records in the Laboratory Notebook in compliance with regulatory guidelines.
- Execute scale-up batches.
- Review CoA and specifications for APIs, RM, and PM.
- Perform Q3 characterization and prepare comprehensive reports accordingly.
- Compile and review essential documents such as BOM, MFC, BPR, and BMR for formulation and development projects.
- Execute both scale-up and exhibit batches.
- Coordinate with the Analytical Development Department, Purchase, and Project Management teams for seamless project execution.
- Liaise with QA, QC, Production, and Technology Transfer teams at manufacturing sites to facilitate smooth scale-up and technology transfer processes.
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