Manage Quality Assurance Activities, Ensuring Quality of the products, GMP & GLP compliance, ISO Compliance - Preparation & Controlling Documents, Records, Master BMR, Prepare protocols for validation, Reviewing documents to identify the gaps, Improving quality parameters, training of QA/QC personnel, sampling, facing audits, leading a team of Q.A professionals and manage allied activities and other related jobs. 
Supervising Manufacturing Activities. To ensure Employee training on GLP, GMP.
To carry out document preparation like SOP, Validation Protocol, Validation Reports, and Validation Summary.
Work experience in Hemo Dialysis Fluid & Concentrates is a plus.
Minimum 3 year experience in Quality Assurance or combination of QA and QC.
Please send all relevant documents scan copy and mention your present and expected salary.