Specialist Quality Control (Technical Resources)
AmgenHyderabad, Telangana, India
Posted February 9, 2026
Full Time
About the Company
Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We helped establish the biotechnology industry, and we remain on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, osteoporosis, inflammatory diseases and rare diseases. Amgen is one of 30 companies comprising the Dow Jones Industrial Average®, and part of the Nasdaq-100 Index®. In 2024, Amgen was named one of the “World’s Most Innovative Companies” by Fast Company and one of “America’s Best Large Employers” by Forbes. For more information, visit Amgen.com and follow us on X, LinkedIn, Instagram, TikTok, YouTube and Threads. 🔗 Community Guidelines: https://wwwext.amgen.com/community-guidelines 🔗Global Privacy Statement Directory: www.amgen.com/dp Special Advisory: Please be cautious of scam recruitment offers claiming to be from Amgen. Such scams may come from various sources, including fake websites and/or unsolicited emails and seek to obtain personal data or payment from victims by offering jobs that do not exist. Please be advised that Amgen would never ask for payment to progress a job application. When in doubt, please check to see if the position in question is posted on this website before applying. Additionally, please report any suspicious recruiting activity to https://complaint.ic3.gov/ and thank you for your assistance.
Job Description
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.
Requirements
- Managing document requests from the global QC Network
- Creating, authoring, revising, and coordinating workflows for controlled document types
- Collecting, organizing, and analyzing data from multiple repositories
- Facilitating information gathering and alignment across the QC Network and cross-functional partners
- Driving project deliverables to ensure timely and high-quality completion of assigned tasks and initiatives
- Supporting issue identification and resolution, collaborating effectively across sites and functions
- Ensuring all controlled documents meet Amgen's quality standards and comply with cGMP, safety, and other applicable regulatory requirements
- Ensuring all assigned training requirements are completed, current, and compliant with cGMP standards
- Identifying opportunities for continuous improvement to ensure alignment in document structure, formatting standards, and data retrieval/compilation practices across the network
Benefits
- Full-time employment
