Amgen Inc
Sr Associate Clinical Supply Chain Support Office
Skills
2 months ago
Share this opportunity
Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.
Important information
Contract type:
Permanent
Location:
Hyderabad, Telangana, India
Work mode:
Onsite
Published on:
17 August 2026
What they need
In this vital role, you will serve as Sr Associate, supporting the Design and Setup of the Clinical Supply Chain.
Reporting to the Manager Clinical Supply Chain - Change Mgt, and directed by the Global Setup Leads, you will contribute to the execution and completion of key deliverables associated with setup activities of global supply chains for clinical trials, by leading information gathering across stakeholders such as RD, Regulatory Affairs, Site Supply Chain and Master data, and task close out.
In close collaboration with the Global Setup Lead team, you will ensure reliable, compliant, and right-first-time process execution, transparent status reporting on progress, and pro-active identification of risks and mitigation strategies for closing out deliverables.
The role is accountable for managing various deliverables such as:
Master data requests for product materials, BOM, and study related attributes in SAP.
Creation of the Clinical Artwork requests and facilitating prioritization of outstanding attributes in relation to the request form.
Creation and maintenance of Product Specification Files, and Depot Plans.
Roles Responsibilities Master Data in ERP (SAP)
Central focus point for ERP (SAP) readiness:
Initiate clinical label material requests;
Requesting Finished Drug Product Materials, Bill of Materials (BOM), Work Breakdown Structure (WBS) elements, Custom Values and ensures timely availability to adhere to overall project timelines
Ensures setup of Study Design Tables.
Setup Activities
Coordinate and prioritize artwork creation process via initiation and routing of clinical artwork creation request forms, facilitating discussions to resolve issues and following up on outstanding queries.
Creates and maintains Product Specification File Study throughout the life cycle of the clinical trial
Creates and maintains third party depot plans and cross docks to support global study footprint
Reporting
Maintains Metrics for Global Setup lead team
Contributes to monthly Workforce planning cycle
Qualifications
5+ Years of experience with Bachelors Bachelor degree or equivalent in logistics, business administration or life science.
Typically relevant working experience, preferably in the biotechnology or pharmaceutical industry,
Typically relevant working experience in an international and regulated environment
Understanding of fundamentals of logistics /supply chain principles (especially BOM)
Experience in planning
Experience in project management techniques
Advanced experience in MS Office applications (Word, Excel)
Fluency in English, both in oral and written communication
High quality standards with regards to work
Ability to set priorities and timely escalation
Other offers great for you!
These companies are also looking for great profiles
Yunik
Data Analyst Senior - Supply Chain
Freelance
Paris, France
Hybrid
Skills
1 day ago
Quick apply
skiils
Digital Product Manager / Product Owner Supply Chain
Freelance
Lille, France
Hybrid
Skills
4 hours ago
Quick apply
Come Together
Chef de projet métier Supply Chain
Freelance
Lille, France
Hybrid
Top Recruiter
Skills
4 hours ago
Quick apply