Associate Scientist

About the role

This position focuses on literature search, idea generation, and preparation of technical reports. The role involves preparing product development strategies for sterile drug products while considering technical, IP, regulatory, and clinical requirements.

Responsibilities

• Screening and selection of raw materials (APIs, excipients, packaging components)
• Pre-formulation and solution chemistry studies
• Process development and optimization for complex injectable development
• Stability evaluation and applicability of QbD principles in product development
• Basic physico-chemical testing and understanding of regulatory framework pertaining to product development and filing (ICH, regulated markets)
• Handling of technology transfer batches and submission in regulated markets
• Following GDP, cGMP, GLP and laboratory safety practices during work

Qualifications

• Doctorate in Pharmaceutical Technology or Polymers
• PhD with 2-3 years experience

Skills

• Multi-tasking capability along with ability to think out-of-the-box
• Good interpersonal skills
• Effective verbal and written communication skills