Fda Approved+./.with Around 12 to 15 Years of Total Experience in Pharmaceutical Company.
overall Responsibility for Application of Quality Management System..
quality Risk Management System as Area Requirements.
review of Training & Audit Records, Vendor Validation.
compliance Record ( Internal & External Audit Report )
current Updation of Site Master File.
recall Alert System Mock Recall Practices, Change Control, Deviation & Oos, Oot
overall Responsibility of Quality Control Lab.
to Ensure the Compliance of Current Laboratory Practices and Standard Operating Procedures in . Laboratory.
to Ensure Testing, Approval or Rejection of Raw Materials, Packaging Materials, Bulk/finished Products.
co-ordination with Micro & Production for Compliance of Inputs and Products with Respect to Chemical / Instrumentation Parameters.
to Ensure the Quality Standards of Raw Material, Semi-finished Product, Finished Products with Respect to Chemical / Instrumentation Parameters.
generation of Qualification Protocol and Execution of Method Validations and other Relevant Chemical / Instrumentation Validation.
investigations of Failures in Environmental Water System & Quality of Product with Respect to Chemical / Instrumentation Parameters.
Experience : 12 - 17 Years
No. of Openings : 1
Education : M.Sc
Role : Quality Control Manager
Industry Type : Pharma / BioTech / Clinical Research
Gender : Male
Job Country : India