Research Associate

• Responsible for all Sterile and Nonsterile products for packaging material new development.
• PIF evaluation and Literature Review for new products
• RLD/Innovator packaging material analysis and preparation of characterization reports
• Preparation of trade dress and packaging Developments reports.
• Proposing primary and secondary packaging materials for new products
• Sourcing of packaging materials and vendor finalization.
• Preparation of Specifications and STP for packaging materials.
• Preparation of master packaging card (MPC)
• Preparation of Bill of materials for packaging materials
• Review of CFT/CMO documents (BPR)
• Preparation of Threshold analysis reports and DHF documents.
• Preparation of protocols for in-house and external lab testing for packaging materials.
• Coordination with CFT teams and customers for smooth documentation.
• Coordination with CMO for smooth execution of Exhibit batches.
• Coordination with suppliers for layout/ change parts development.
• Preparation of Packaging Development SOP’s
• Initiating Change Controls for documentation.
• Preparation of bracketing sheets for container closure system and generation of protocol-based packaging functionality studies and design qualification studies.

Diploma In Packaging Technology with 4 to 6 years of experience in R&D pharmaceutical packaging Development