Name: Jobpe
Address: T-Hub, Plot No 1/C, Sy No 83/1, Raidurgam panmaktha, Knowledge City Rd, Hyderabad, Telangana, 500081, IN
Telephone: +91-83339-09630
Price range: Free

Quality Control Analyst II Teva Pharmaceuticals

11.0 - 15.0 years

0 Lacs

chennai

On-site

Role Overview: As a Quality Control Analyst II at Teva Pharmaceuticals, you will be responsible for performing Stability analysis, Method transfer, Method Validation, and reviewing analytical documents. Your main tasks will include preparation and review of Method Transfer Protocols (MTP), Method transfer report (MTR), Method of analysis (MTH), Standard Testing Procedure, Test Data Sheet (TDS) 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. Additionally, you will be involved in the review and maintenance of all logbooks of the...

Posted 1 week ago

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QMS Incharge Syngene International Limited

9.0 - 13.0 years

0 Lacs

karnataka

On-site

Role Overview: As a Deputy Manager at Syngene International Ltd., your main responsibility will be handling QMS documentations like CC, CAPA, and Investigations, as well as managing EDMS documents, study protocols, and qualification protocols. You will be in charge of performing activities related to Engineering & maintenance at Biologics Unit 03 while ensuring GMP compliance and error-free operations. It will be crucial for you to follow all EHS requirements at the workplace to ensure individual and plant safety. Key Responsibilities: - Handling QMS documentations like CC, CAPA, and Investigations - Managing EDMS documents, study protocols, and qualification protocols - Performing activitie...

Posted 1 month ago

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QMS Incharge Syngene International Limited

9.0 - 13.0 years

0 Lacs

karnataka

On-site

As a Deputy Manager at Syngene International Ltd., your main responsibility will be handling QMS documentations like CC, CAPA, and Investigations, as well as managing EDMS documents, study protocols, and qualification protocols. You will be in charge of performing activities related to Engineering & maintenance at Biologics Unit 03 while ensuring GMP compliance and error-free operations. It will be crucial for you to follow all EHS requirements at the workplace to ensure individual and plant safety. - Complete all assigned mandatory trainings related to data integrity, health, and safety measures on time - Ensure compliance to quality systems and current good manufacturing practices - Develo...

Posted 3 months ago

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