Vendor Management - Assocciate Manager /Manager Zydus Group

5.0 - 9.0 years

0 Lacs

ahmedabad, gujarat

On-site

As a member of the Central Quality department, your role involves: - Conducting Vendor Audit & Compliances - Reviewing Procurement bill of material (PBOM) - Initiating and evaluating change control, Corrective and Preventive Actions (CAPA) through track wise software - Evaluating Certificate of Suitability (CEP) updation, Drug Master File (DMF) notification, and Vendor notification for implementation at formulation sites - Reviewing Quality Management System (QMS) documents of all sites - Auditing formulation sites as per self-inspection plan - Preparing Audit planner for Active Pharmaceuticals Ingredients, Excipients, packing materials, Key Starting Materials (KSM)/Intermediates, Sterile ar...

Posted 1 week ago

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Global Engineering UPS Referent Schneider Electric

5.0 - 9.0 years

0 Lacs

karnataka

On-site

As the Global UPS Referent for GCP-OPS within Global Systems Engineering & Expertise at Schneider Electric, your role involves bringing a high level of technical expertise to major electrical infrastructure projects for international customers. You will be responsible for ensuring the right level of technical knowledge for tenders and the execution of complex projects. Your primary duties include securing complex tenders and projects, managing the technical referential, leading the technical community, supporting technical management, ensuring technological watch, and assessing technical knowledge. To excel in this role, you should possess a high level of knowledge and experience in customiz...

Posted 2 months ago

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QMS Project Reviewer Syngene International Limited

3.0 - 7.0 years

0 Lacs

karnataka

On-site

Job Description: As a QMS Project Reviewer at Syngene International Limited in Bengaluru, you will play a vital role in drug substance development and manufacturing processes. Syngene is an innovation-led contract research, development, and manufacturing organization that offers integrated scientific services from early discovery to commercial supply. Safety is a top priority at Syngene, and you will be expected to adhere to safety guidelines, procedures, and SOPs to ensure a safe working environment for yourself, your team, and the lab/plant. Your core responsibilities will include following GMP, GDP, and GLP procedures, creating/revising/reviewing procedures such as SOPs and protocols, rev...

Posted 3 months ago

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