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Countries
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This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Lead the acquisition and quality management of non-CRF clinical trial data as Data Acquisition Lead in Hyderabad, India. This role requires 8+ years of clinical execution experience, including vendor oversight and global trial delivery. You will ensure timely, compliant data ingestion, drive auto...
Study Delivery Senior Associate needed in Hyderabad, India to support global clinical trial execution. You will partner with Study Managers, lead study trackers, dashboards, and vendor logistics while managing start-up activities and risk monitoring. Requires a Master’s degree or equivalent clini...
Join Amgen in Hyderabad as a Regulatory Statistical Programming expert. Leverage your SAS, R, or Databricks skills to support real-world evidence (RWE) generation for regulatory submissions. Ideal for professionals with a Bachelor’s in a scientific field and 2+ years of life sciences programming ...
Seeking a **Study Data Delivery Manager** in **Hyderabad, India** to lead end-to-end clinical data management. You will ensure high-quality, decision-ready data by driving the Data Management Plan, overseeing database build, and managing study conduct activities. Ideal candidates have a life scie...
Lead C&Q documentation preparation for Drug Product systems at Amgen in Hyderabad. This role requires 8-13 years of GMP commissioning and qualification experience in pharma or biotech. You will manage a blended team, overseeing protocols, risk assessments, and traceability matrices for global Eng...
Manager, C&Q Document Preparation (Finished Drug Product / Packaging)
Lead C&Q documentation preparation for Finished Drug Product and packaging systems at Amgen in Hyderabad. This role manages a blended team, ensuring compliant, inspection-ready protocols and reports for GMP manufacturing and capital projects. Requires 8-13 years in pharmaceutical commissioning/qu...
Seeking a skilled Reltio MDM Developer to join us as Associate, Data Management in Hyderabad. You will design scalable MDM solutions, leveraging expertise in Lifecycle Actions (LCA), Java, and API integrations. Ideal candidates have 2-5 years of experience, strong SQL/Python skills, and Pharma/Li...
Lead C&Q documentation for major biotech projects in Hyderabad. Manage a team preparing GMP qualification protocols and reports for drug substance manufacturing systems. Requires 8+ years in pharma validation and strong leadership experience. Ensure compliance and operational readiness in a dynam...
Manager, C&Q Document Preparation (Facilities and Utilities)
Lead C&Q documentation for pharmaceutical facilities and utilities at Amgen's Hyderabad site. Manage a team preparing compliant, inspection-ready protocols and reports. Requires 8+ years in GMP commissioning/qualification and team leadership. Ensure project success in a dynamic, cross-functional ...
Senior Associate Supply Chain Compliance Management role in Hyderabad, India. Ensure GMP compliance, manage SOPs, and lead documentation for Amgen's external manufacturing network. Requires 5-9 years' supply chain experience in pharma/biotech, strong GMP knowledge, and audit support skills. Drive...
Amgen seeks a Senior Associate Supply Chain Planner in Hyderabad, India, to join its External Planning Team. This role ensures data integrity and accurate execution of external supply plans using SAP and Kinaxis RapidResponse. Ideal candidates have 5-9 years of supply chain experience in a regula...
Lead statistical programming for global clinical studies as a Biostatistical Programming Manager at Amgen in Hyderabad. You will serve as Study Lead Programmer, managing end-to-end deliverables, ensuring CDISC SDTM/ADaM compliance, and supporting regulatory submissions. Requires 6+ years of exper...