Quality Assurance Inspector- GLP MS CLINICAL RESEARCH

8.0 - 12.0 years

0 Lacs

karnataka

On-site

As an experienced Quality Assurance (QA) professional with expertise in ICH-GCP and GLP principles, your role at MSCR will be crucial in ensuring the highest standards of quality and compliance across clinical research and laboratory operations. You will be responsible for developing and maintaining ICH/GCP-compliant processes, leading internal quality audits, conducting study audits, and driving continuous quality improvement initiatives. Your role will also involve ensuring GLP compliance, managing documentation and SOPs, overseeing study conduct, and liaising with regulatory authorities. Key Responsibilities: - Develop and maintain ICH/GCP-compliant processes for controlling the quality o...

Posted 3 weeks ago

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Quality Assurance Inspector- GLP MS CLINICAL RESEARCH

8.0 - 12.0 years

0 Lacs

karnataka

On-site

As an experienced Quality Assurance (QA) professional with 8-10 years of experience in clinical research, pharmaceuticals, or life sciences, you will play a crucial role in ensuring the highest standards of quality and compliance at MSCR. Your expertise in ICH-GCP and GLP principles will be essential to maintain regulatory guidelines, clinical QA processes, and GLP compliance throughout the organization. Key Responsibilities: - Develop and maintain ICH/GCP-compliant processes to control the quality of work and clinical studies at MSCR. - Lead and manage internal quality audits, CAPA activities, and quality management reviews. - Conduct study audits to ensure adherence to sponsor protocols, G...

Posted 3 months ago

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Clinical Trial Manager Vopec Pharmaceuticals (P) Ltd

10.0 - 14.0 years

0 Lacs

chennai, tamil nadu

On-site

As the Manager of Clinical Trials at Vopec Pharmaceuticals Private Limited, a pioneering biotech company specializing in oncology, you will play a crucial role in leading the execution of Phase II studies for the lead program AB001, targeting PD-L1 and multiple cancer pathways. This role offers a rare opportunity to work on cutting-edge cancer therapeutics and make a significant impact on patient lives globally. Your key responsibilities will include developing and implementing comprehensive clinical trial plans and protocols in compliance with regulatory guidelines, managing clinical trial sites and investigators, overseeing all aspects of Phase II trials, including patient recruitment and ...

Posted 4 months ago

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