TIEFENBACHER PHARMACEUTICALS is in-house developing, manufacturing, and commercializing generic, value added, and innovative pharmaceutical products worldwide Driven by our purpose of bringing high-quality medicines within affordable reach to patients around the world, we provide over 180+ products across various therapeutic categories in 10+ dosage forms – and additional medical devices and drug device combinations with integrated e-health solutions.
Post : Dy. Manager / Manager
Department : Development Quality Assurance
Experience : 12 to 15 Years
Qualification : M. Pharmacy / B. Pharmacy / Any relevant
Job Description
• Responsible for review and approval of Method validation, Method transfer, Stability, Test methods, Specifications, Analytical technical documents (ATD's), Working standard qualifications, Instrument/ Equipment calibration reports
• Responsible for investigations related to Laboratory incidents, OOS, OOT, OOE, failure investigations and participating/ involving in these investigations
• Responsible for review and approval of Process development documents like Master Product Card, Reference Formula Card, Study medication batch records, Product development reports & Batch selection reports.
• Responsible for impact assessment & coordination of Change controls and Deviations of Analytical and Product Development Laboratories.
• Responsible for review of audit trials in Analytical Development Laboratory.
• Responsible for compilation of Technical Data Package, Nitrosamine Risk Assessment and ICH Q3D elemental impurities risk assessments.
• Responsible for review and approval of SOP's and Formats related to Quality Assurance, R&D activities
Send your resume at : k.surendra@tiefenbacher.com
Last Date : 10th November 2025
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