Specialist Quality Control (Technical Resources)

In this vital role, you will be part of Amgen India’s (AIN) Quality Control (QC) Technical Resources team, supporting Amgen’s global Quality Control network. The QC Technical Resources team will provide centralized document management expertise across global QC functions, ensuring the efficient, compliant, and consistent management of controlled documents within Amgen’s enterprise document management system. As a QC Specialist, you will be responsible for end-to-end document lifecycle management, including document creation, authorship, review, and revision, for a range of QC processes. These include, but are not limited to, general laboratory practices related to Cell Biology, Chemistry, Microbiology, Biochemistry, and Immunology, laboratory consumables and equipment management, and periodic trend assessments. This position offers a unique opportunity to collaborate with QC teams across Amgen sites worldwide, contributing to process harmonization and continuous improvement. You will gain broad exposure to Amgen’s diverse product portfolio and processes throughout the product lifecycle. This candidate will primarily work a shift-based schedule to enable the business in delivering Amgen’s mission to serve patients. The candidate may need to work outside of his/her routine workday to support business needs. The individual will be required to work from our office located in Hyderabad, India (Amgen India-AIN), and provide remote support from AIN to Amgen sites across multiple time zones globally.