Associate R&D Supplier Management
Amgen
Full time- 2+ years
- Not Disclosed
- Hyderabad, India
- Post Date: Jul 27, 2026
- End Date: Sep 27, 2026
- 2+ years
- Not Disclosed
- Hyderabad, India
- Post Date:Jul 27, 2026
- End Date: Sep 27, 2026
Skills:
- pharma
- pharmacovigilance
- Management
Job Description:
Responsibilities
- Perform general data management and project management activities across multiple verticals.
- Provide transactional study planning and lifecycle support
- Monitor our planning tool for new studies and updates to existing studies
- Assign Planisware number and manage timelines (eg Bioanalytical lab name, PO#, study status)
- Monitor/manage/query key systems to support documentation, planning and forecasting
- Ensure finalized study documentation is archived appropriately
- Support risk management through collection and analysis of metrics, trends and databases.
- Support visualization dashboards, curate content, provide real-time updates
- Pull upcoming studies from MSL systems to support planning and forecasting.
- Generate key shipping documents including international commercial terms, import permits, letters of authorization and others as needed
- Manage procurement and shipment requests (eg critical reagents and study samples)
- Liaise with external suppliers to plan and coordinate key shipments and deliverables
- Perform review and submission of regulated documents and data (eg MVP, MVR, deviations)
- Populate key trackers (eg timelines, purchase orders, supplier issues)
- Monitor CRO reagent trackers and review periodically for accuracy and expiry management.
- Assist in documenting supplier oversight activity (eg evaluation, monitoring, and remediation events)
- Ensure clear communication of progress against all deliverables and prompt escalation of issues.
Qualification & Experience
- Bachelor’s degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, Business Administration, Supply Chain, or a related discipline.
- 2 - 4 years of experience in supplier management, project coordination, study operations, clinical research, laboratory operations, or a related field.
- Experience working with databases, planning tools, and document management systems.
- Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.
- Proficiency in Microsoft Office Suite, particularly Excel, PowerPoint, and database applications.
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Salary
Not Disclosed
-
Role
Associate
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Area of Practice
- Quality Assurance/ Quality Control
-
Experience
2+ years
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