Analysis of Innovator/RLD samples for US, EU, Domestic, and ROW markets.
Preparation of Container Suitability Report and development for the Suitable packaging material for solid Orals and Dry Syrups Products based on R & D Stability Data.
Support to Change Parts Development and Coordination for Machine Trial.
Documents Preparation includes AIF to generate the pack codes, Preparation of Specifications/ General test procedure of packaging materials and PM BOM’s for exhibit batches.
Checking and approvals for Label artworks, Digitals and Multiups received from suppliers.
Permeation Evaluation and Data Preparation of Primary Blister Packaging Materials at Manufacturing Sites.
Support to the Purchase team for alternate vendor development.
Working with SCM system for inventory control for Exhibit batches and execution of exhibit batches at manufacturing Sites.
Desired Candidate Profile:
Graduate with a professional Degree/Diploma in Packaging from IIP or any other reputable Institute with 5-7 years of experience in handling Pharma packaging Materials for regulated markets (US and EU).
Good understanding of primary and secondary packaging material for different dosage form including Solid orals, Semisolids, Liquid oral, Ophthalmic, and Injectables.
Should have basic knowledge about regulatory requirements of different markets for artwork creation.
Technical report writing skills, strong communication and presentation skills.
