ADL

Method development & validation for tablets, capsules, creams & ointments. Exposure to US/EU regulatory requirements.

M.Sc/ B.Pharm / M.Pharm. To plan, prepare and review of high quality dossier with support and guidance, assuring technical concurrency and regulatory compliance, meeting agreed upon timeline.

M.Pharm. Exposure in EU/ US/ UK/ ROW market. Formulation patent exposure. Strong communication skills, Problem-Solving, & Adaptability.

Solid Oral Formulation Development, QbD, Scale-Up, Pilot Batches & Tech Transfer. Literature Review & Excipient Compatibility.

The candidate should competent and motivated in Production (OSD) with sound experience in Oral Solid Dosage manufacturing processes.

HOF Pharma was founded with the idea of reaching the forefront of pharmaceutical industry. Built on the foundation of hope and care

Experience in Blister Line, Bottle Line, QMS, Documentations. Can able to Manage shift operation Independently.

To carry out development trials for the allocated project in formulation laboratory along with online recording of experiments and data compilation.

Analytical method development of finished dosage forms. Stability studies of finished dosage forms. Analytical method validation Analytical method transfer.