Teva Pharmaceutical Industries Ltd. is an Israeli multinational pharmaceutical corporation. Teva’s main focus is on generic drugs, although the company also has investments in branded drugs, active pharmaceutical ingredients, contract manufacturing services, and an out-licensing platform.
Teva Pharmaceuticals is hiring a Quality Control Analyst for Formulation Pharmaceuticals. Responsibilities include stability analysis, method validation, instrument calibration, and SOP preparation. Join us today!
Quality Control Analyst (Formulation Pharmaceuticals)
Your experience and qualifications
M.Sc (Chemistry) with 5 to 10 years of experience
Job description
- Performing Stability analysis and review of documents.
- Performing Method transfer/ Method Validation
- Calibration and validation of instruments / equipments.
- 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 guidelines.
- Preparation of departmental SOPs in compliance with current guidelines.
- Preparation of validation protocols in compliance with current guidelines.
- Entry of stability sample results in LIMS.
- Handling of LSCMS Software.
Reports To
Group Leader Quality Control
Work Location
Chennai, India, 600113
Interested candidates click here to apply online
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