2 Ivd Documentation Jobs

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6.0 - 10.0 years

0 Lacs

surat, gujarat

On-site

As an experienced professional with a minimum of 6-8 years in Quality assurance and regulatory, this opportunity is tailored for you. With a background in Graduate or Post Graduate studies in Pharmacy, Biochemistry, Biotechnology, or Chemistry, you are well-equipped to excel in this role. Your knowledge of techniques involving quality assurance of pharmaceuticals antibodies/Proteins, along with on-job experience in in vitro MDD/IVD documentation, will be valuable assets. **Key Responsibilities:** - Monitor Implemented Quality Control Systems - Provide training wherever required - Conduct Internal audits at regular intervals - Coordinate Batch failure and OOS Investigations ensuring appropria...

Posted 4 weeks ago

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6.0 - 10.0 years

0 Lacs

surat, gujarat

On-site

Role Overview: You should have a minimum of 6-8 years of experience in Quality assurance and regulatory, preferably in the field of pharmaceuticals, antibodies, proteins, IVD/medical devices, or injectables. As a Graduate or Post Graduate in Pharmacy, Biochemistry, Biotechnology, or Chemistry, you will be responsible for ensuring the quality control systems are implemented effectively and participating in various quality assurance activities. Your innovative thinking and leadership skills will be crucial in solving problems related to the Quality Management System. Key Responsibilities: - Monitor and ensure the implementation of Quality Control Systems - Provide training as and when required...

Posted 3 months ago

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