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).
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 ...
Location
India , Hyderabad
Salary
Not provided
Amgen
Expiration Date
Until further notice
Study Data Deliver Mgr
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...
Location
India , Hyderabad
Salary
Not provided
Amgen
Expiration Date
Until further notice
Manager, C&Q Document Preparation (Drug Product)
Location
India , Hyderabad
Salary
Not provided
Amgen
Expiration Date
Until further notice
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...
Location
India , Hyderabad
Salary
Not provided
Amgen
Expiration Date
Until further notice
Reltio Developer
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...