Support new product and technology transfer activities. Review and approve tech transfer documentation. Coordinate with Production, QC, R&D, and Regulatory teams.
Support development, optimization, validation and transfer of analytical methods using Mass Spectrometry techniques for pharmaceutical products and materials.
Green Field Project -Equipment Qualification & Computer System Validation, HVAC, Water System, Compressed Air, Nitrogen system Qualification & Temperature Mapping.
Support compliance documentation activities related to computer systems, including review coordination, evidence collection, document quality checks, and maintenance of controlled documentation.
Drive for self-development, the ability to collaborate, and an action-oriented work ethic. Strong communication skills with the ability to distil complex information into clear, actionable insights for clients.
BDR Pharmaceuticals International Pvt Ltd and BDR Life sciences Pvt. Ltd, each one having stamped its own supremacy in respective fields, i.e. API and formulation manufacturing, respectively.
B.Sc. degree in Life Science/Pharmacy or equivalent/related discipline or certification in a related allied health profession from an appropriately accredited institution