3 - 5 Years
Responsible for all instrumental and chemical analysis of finished product & Intermediates samples.
Responsible for handling external & internal audits and audit responses.
Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations.
investigating and setting standards for quality/health and safety
Responsible for Maintaining documents as per ISO & GMP guidelines.
Review and approve of analytical documentation such as specifications,
test methods, analytical records, stability protocols, stability reports,
training documents, investigation reports and equipment qualification
Responsible to identify area for improving quality of work and suggest
maintain all the instruments / equipments in calibrated & operating condition on or before due.
To conduct the activity of preparing working standards, procuring new reference standard as well as reference cultures and maintains all the records of same as per SOP.
To prepare document and maintain the quality system as per procedure and provide support to plant during regulatory inspection.
|Salary||2 Lac To 4 Lac P.A.|
|Industry||Pharma / R&D / Biotech|
|Work Experience||3 - 5 Years|
jay maharaj job placement
|About Company||We are placement Consultant and we provide exp. Candidates as per Company Requirements.|
|Contact Person||Ms. Nikita|