Manager - API Dishman Carbogen Amcis Ltd

0.0 years

0 Lacs

india

On-site

Title: Manager - API Custom Field 2: 2779 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Preparation and review of Standard Operating Procedures. Issuance, review of OOS,OOT,Deviation,CAPA,Change Control & its Management. Handling and monitoring of control samples. To impart internal trainings to DCAL Employees. Review of Calibration records, Instrument Logs of Quality Control. To Review of Analytical Method Validation protocols and reports. Review of the Instrument qualifications and re-qualifications protocols of Quality control. Preparation & review of quality risk assessment docume...

Posted 3 days ago

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Quality Analyst I Teva Pharmaceuticals

5.0 - 7.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with. How You...

Posted 1 month ago

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QA Executive Capital Placement Services

4.0 - 10.0 years

3 - 6 Lacs

bharuch, gujarat, india

On-site

Manage release of product batches, including owning the QA product release workflow in SAP. Lead and supervise a team of QA professionals to perform operations as described. Review and approve Deviations and Laboratory Investigations. Review and approve Purchase Specifications and Analytical Standards. Review and approve Issue Reviews and CAPA. Assist with Non-Conformance Investigations and provide guidance in identifying potential product impact and determination of final product disposition. Review and update Standard Operating Procedures (SOPs) for GMP compliance. Follow all regulatory guidelines, cGMP guidelines, Environmental Health and Safety regulations as required. Review validation ...

Posted 1 month ago

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Sr. Manager, Quality Control - Chemistry & Device Lilly

5.0 - 9.0 years

0 - 0 Lacs

haryana

On-site

At Lilly, you will play a crucial role in ensuring the safety and efficacy of drug and device products by leading a team of laboratory personnel in performing routine and non-routine testing. As the Sr. Manager, Quality Control (QC) Chemistry and Device, your responsibilities will include scheduling and planning laboratory activities, reviewing laboratory data, and providing technical support for laboratory projects. You will oversee the onboarding of laboratory instrumentation and equipment, manage personnel learning plans, and utilize your technical expertise in inspection/audit activities and continuous improvement initiatives. Your key objectives will involve leading a team of laboratory...

Posted 1 month ago

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