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Teva Pharmaceuticals has been developing and producing medicines to help improve people’s lives for more than a century. We are committed to being a global leader in generic and specialty medicines with a portfolio of 3,500 products in nearly every therapeutic area. Around 200 million people around the world take a Teva medicine every day. They are served by one of the largest and most complex supply chains in the pharmaceutical industry. Along with our established presence in generics, we have significant innovative research and operations supporting our growing portfolio of specialty and biopharmaceutical products. Learn more at www.tevapharm.com. Please note that adverse effects for any of our products should be reported to: Safety.AE@teva.co.il Product-specific questions should be directed to Teva or Teva Group subsidiaries in your country. Contact details and Teva's Pharmacovigilance Privacy Policy may be found here: http://www.tevapharm.com/contact_us/
Not specified
INR 2.0 - 5.0 Lacs P.A.
Work from Office
Full Time
Job Description:Performing Stability Analysis.Performing Method transfer/ Method Validation Analysis.Calibration and validation of instruments / equipment's Analysis.Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelinesPreparation of departmental SOPs in compliance with current guidelines.Preparation of validation protocols in compliance with current guidelines.Entry of stability sample results in LIMS / SAP.Handling of LSCMS Software.
Not specified
INR 6.0 - 10.0 Lacs P.A.
Work from Office
Full Time
Job Description:Performing Stability analysis, Method transfer and Method Validation.Preparation and review of Method Transfer Protocols, Standard Testing Procedure, Test Data Sheet for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports and any document related to stability analysis, method transfer and method validation in compliance with current guidelines. Review and maintenance of all logbooks of the departmentPreparation of departmental SOPs in compliance with current guidelines. Review of departmental SOPs, training of analysts and other technical staff and review validation of data transfer, data management using computer systems.Preparation and review of validation protocols in compliance with current guidelines.Calibration and validation of all instruments / equipments. Procurement of columns, chemicals/ reagents/ solvents and standards for various stability analysis, method transfer and method validations.
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
INR 0.0 - 0.0 Lacs P.A.
Work from Office
Not specified
Not specified
INR 0.0 - 0.0 Lacs P.A.
Work from Office
Not specified
Not specified
INR 0.0 - 0.0 Lacs P.A.
Work from Office
Not specified
Not specified
INR 0.0 - 0.0 Lacs P.A.
Work from Office
Not specified
Not specified
INR 12.0 - 22.0 Lacs P.A.
Work from Office
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
INR 6.0 - 9.0 Lacs P.A.
Work from Office
Full Time
Not specified
INR 3.0 - 6.0 Lacs P.A.
Work from Office
Full Time
Not specified
INR 5.0 - 9.0 Lacs P.A.
Work from Office
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
Not specified
0.0 - 0.0 Lacs P.A.
On-site
Full Time
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