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. â€¨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.