Job Description
Job Title:  Dy Mgr-Technical Services
Req Id:  966
Posting Start Date:  10/21/26
Job Description: 
  • Successful Scale-up for new molecule from Lab to pilot scale and commercial scale.
  • Basic engineering for new product commercialisation or capacity enhancement projects or environment management system.
  • Review of basic engineering package for capacity enhancement which includes capacity calculation, Process block diagram, Equipment sizing, Utility calculation etc.
  • Capex estimation. 
  • Coordinating with Vendors/Consultants for various deliverables at different stages of the Project. 
  • Review and approve of P&IDs, Lay out, technical specification, Vendor / Consultant documents for the projects. 
  • Review and approve of Qualification documents such as URS, Design Specification, FRS, DQ, IQ and OQ. 
  • Commissioning support & product deliverables. 
  • De-bottlenecking of existing capacity and proposal for Capacity enhancement. 
  • Collaborating Cross functional team for new process validation and commercialization. 
  • Identification and implementation of new technologies for various unit operations. 
  • Performance evaluation of the systems and supporting various cost effective, energy conserving process engineering activities of the department.      
  • Supporting R&D for technology development. 
  • Guide the team for resolution and smooth execution. 
  • Identification of improvements in existing process followed by implementation in pilot plant and commercial plant with collaboration with R & D.
  • Review of the equipment’s mapped for New Products and Plan for the Modifications/Resources in coordination with manufacturing team. 
  • Review and Approve the process outlines and plan for the scale up and validations 
  • Review and Approve of Equipment equivalence reports, Scale-up reports, Validation Protocol, Validation reports, Cost reports and other Pilot Plant and Technology transfer related documents. 
  • Trouble shooting & investigation of Scale-up related Problems, Routine commercial OOS/OOT’s by identifying root causes and suggesting Corrective and Preventive action to avoid failure, deviations and change controls through Track wise system. 
  • Coordinate during internal & external audits and ensuring compliance with respect to Quality system. Submission of relevant data for DMF filing. 
  • Driving Task force activities/ Key continuous improvement initiatives with respect to yield improvement, solvent recovery.
  • Prepare and review CRDMO costing with necessary inputs as per project management / customer requirement.