4.0 - 6.0 years

8 - 13 Lacs

Hyderabad, Telangana, India

On-site

About the RoleMajor Accountabilities: Manage the operational aspects of CROs supporting Novartis BR scientific functions and projects under the supervision of ORE team members. Drive efficient, cost-effective, high-quality infrastructure and logistics for outsourcing scientific activities, including invoice reconciliation, sample retention logistics, data QC, process automation, and scientific material stewardship. Act as the scientific contact for the operation and logistics of outsourcing requests. Collaborate with scientific functions to ensure assay performance and data QC. Gather input and provide recommendations for optimizing resource allocation; identify issues and propose mitigating...

Posted 1 month ago

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Project Management Coordinator–Documentation Management Amgen Inc

1.0 - 3.0 years

3 - 6 Lacs

Hyderabad

Work from Office

What you will do In this vital role you will the Project Management Coordinator will play a key role for the management of Research & Documents controlled documents through helping to strengthen and advance Amgens R&D Quality Management System. This role contributes to implementing strategies and to ensure excellence in R&D controlled document management. Roles & Responsibilities: As an integral team member working globally with R&D Quality team members and R&D Business Process Owners to ensure compliance with GCP regulations and other requirements: Provide technical writing and editing expertise to support the generation of robust, well-written R&D controlled documents. Coordinate workflows...

Posted 3 months ago

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GCP Quality Compliance Manager Amgen Inc

4.0 - 6.0 years

7 - 10 Lacs

Hyderabad

Work from Office

What you will do The Quality Compliance Manager is a global role and part of the Process Quality team for the R&D Quality Organization. In this vital role you will work with a team of process-focused colleagues who work to complete Amgens Process Quality strategy, which is vital to ensuring that Amgens Research and Development Standards (SOPs and associated documentation) are adequate, clear, and up to all applicable current regulations and quality requirements. The R&D Process Quality team supports the Quality Management System (QMS) across all areas of research at Amgen, including discovery through the full clinical development lifecycle. This team ensures that all Amgens business procedur...

Posted 3 months ago

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