1, responsible for research and development management, control research program, monitor the progress of research to ensure that the research process of norms, science, compliance; 2, to participate in project research, the feasibility of new projects and the difficulty of making recommendations; 3, to ensure that the project can be carried out on a timely basis to maintain the quality of durability; 4, all ...
Handling Change Control & Deviation incident Reports To review and complete Lot mfg. record (LMR) and Batch pkg record (BPR).Reconciliation of packing &manufacturing stage yield. Preparation, revision & distribution & control of necessary documents r
- Lead the Commercial and R & D Procurement Functions - Lead the National and International Planning and Logistics functions - Running the Cost Engineering Programs - Budgeting and Planning - Identify and implement continuous improvement initiatives to enhance capacity utilization
KLIND/ KLAP testing facility, to improve test methodologies - Contribute ideas for innovation projects such as new lubricant concepts in current application and with OEM's to the R&D and contribute technically tWork on-site with customers to solve maintenance and production issues, helping to improve
on supports like carbon, alumina, SiO2 for applications in pharmaceuticals chemicals, agrochemicals.- Exposure to catalyst characterization and evaluation techniques: surface area, pore size, pore size distribution, dispersion of metal particles, size of metal particles, pulse chemisorption, spectroscopic
their operations in Russia, CIS, Europe, USA and Indian markets.Job Description :SUMMARY OF THE OVERALL JOB :- To manage R&D projects as per predefined time, quality and cost basis which are signed in SRC goal sheet - To ensure product launch as per NPL calendar (w.e.f. 01 Nov 15) KEY RESULT AREAS - Projects
the solution/service. Should have proactive approach for R&D project management Should have experience of activities related to formulation development/analysis related to oral solid dosage forms, probiotics, syrups, injections, topical etc. Should have knowledge of ICH guidelines for stability studies Should have
To conduct independent literature investigation to define an appropriate basis for analysis To conduct method development activities as directed in a timely and efficient manner To document development activities, draft specifications and procedures as appropriate To use various laboratory equipment for method development, method validation and routine sample analyses, such as HPLC, UPLC, LC-MS/MS ...