5.0 - 9.0 years

0 Lacs

indore, madhya pradesh

On-site

Role Overview: As a Block Head at our injectable manufacturing facility, you will lead a key production block. Your main responsibilities will involve overseeing end-to-end manufacturing operations, managing a team of production staff, driving process optimization, ensuring regulatory audit readiness, maintaining compliance with cGMP standards, implementing changes, overseeing equipment and maintenance, coordinating cross-functionally, and managing inventory and resources. Key Responsibilities: - Oversee end-to-end manufacturing operations - Manage a team of production staff - Drive process optimization - Ensure regulatory audit readiness - Maintain compliance with cGMP standards - Implement...

Posted 14 hours ago

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Scientist II, Bioanalytical The U.S. Pharmacopeia (USP)

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

At USP, inclusive scientific collaboration is highly valued as it is believed that diverse expertise enhances the development of trusted public health standards. The organizational culture at USP promotes equitable access to mentorship, professional development, and leadership opportunities to ensure broad participation in scientific leadership for stronger and more impactful outcomes in global health. As an equal employment opportunity employer (EEOE), USP is committed to fair, merit-based selection processes that allow the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Accommodations are provided to individuals with disabiliti...

Posted 1 week ago

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PMO Lead Tool Validation & QMS Automation Olympus Medical Systems India Pvt Ltd

5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

As a PMO Lead specializing in Tool Validation & QMS Automation, you will be responsible for driving tool validation projects, automating validation processes, QMS documentation automation, and exploring productivity-enhancing tools in the Engineering Operations of the Digital Unit. Your role is pivotal in ensuring compliance with regulatory standards such as FDA, ISO 13485, IEC 62304, and IEC 82304-1 while promoting innovation and operational efficiency within engineering and quality processes. Your key responsibilities will include owning and managing the lifecycle of tool validation projects, developing and maintaining validation plans, protocols, and summary reports, implementing automate...

Posted 1 month ago

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