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Job Location | Chennai |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Pharma / Biotech |
Functional Area | General / Other Software |
EmploymentType | Full-time |
Teva is a global pharmaceutical leader and the world s largest generic medicines producer , committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success , with colleagues in over 80 countries delivering the world s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient - centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development , marketing , business development and innovation. This is how we improve health and enable people to live better , healthier lives. Join us on our journey of growth! Job Description Performing Stability analysis and review of documents.Performing Method transfer / Method Validation.Calibration and validation of instruments / equipmentsPreparation of Method Transfer Protocols (MTP) , Method Transfer Report (MTR) , Method of analysis (MTH) , Specifications (SPEC) , Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation , Analytical Report (AR) any document related to stability analysis , method transfer / method validation in compliance with current guidelines.Preparation of departmental SOP s in compliance with current guidelinesPreparation of validation protocols in compliance with current guidelines Qualifications Must have 1 - 2 years of work experience in Quality Control FormulationsMust be a Post Graduate in Industrial Chemistry / B.Pharm or M.ScMust possess good communication skills and be performance drivenShould have knowledge of dissolution tester with auto sampler , UV - Visible spectrophotometer , HPLC with Empower 3 software Function Quality Sub Function Manufacturing Quality Control Reports To In process of validation Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas global policy that equal employment opportunity be provided without regard to age , race , creed , color , religion , sex , disability , pregnancy , medical condition , sexual orientation , gender identity or expression , ancestry , veteran status , national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. ,
Keyskills :
inspectioncalibrationqualitycontrolqualityassuranceresearchdevelopmenttestdataqualemploymentopptunitycontinuousimprovementfacilitationmusicmakingglobalpolicymethodtransfermethodvalidatio