Amgen - India, Hyderabad, Quality Control

Senior Associate Quality Complaints role in Hyderabad, India. You will own the end-to-end global complaint process, ensuring compliance with quality standards and regulatory requirements. Ideal for candidates with 4-9 years of Quality experience in biotech or pharmaceuticals, skilled in complaint...

Join Amgen in Hyderabad as an Associate Product Quality - Data Verification. Ensure GMP compliance and data integrity for late-stage products by reviewing critical documents in systems like Veeva and LIMS. Ideal for detail-oriented professionals with 3+ years in pharma and strong GMP knowledge. C...

Associate Quality Complaints role in Hyderabad, India. Manage the global end-to-end complaint process and QMS for a pharmaceutical leader. Ideal for candidates with a Bachelor’s degree and 2+ years in Pharma/Life Sciences. Drive complaint records to closure, ensure SOP compliance, and support qua...

Amgen seeks a Manager - Stability in Hyderabad, India, to lead GMP-compliant stability programs for late-stage and commercial products. This role requires a Master’s in a pharmaceutical science with 10+ years of Quality experience, managing teams and digital GMP systems like Veeva. You will super...

Amgen seeks a Specialist QA, Global Supply Quality in Hyderabad, India. You will ensure high-quality raw materials and devices by collaborating with global teams and external suppliers. The role requires a Master’s with 10+ years or Bachelor’s with 12+ years in cGMP manufacturing and quality syst...

Amgen seeks a Sr. Associate Quality Complaints in Hyderabad, India, to join the Product Complaints and Surveillance team. This role manages end-to-end global complaint investigations, ensuring compliance with quality standards and regulatory requirements. Ideal candidates possess a Master’s degre...

R&D Clinical Quality Compliance Senior Manager sought in Hyderabad, India. This role provides proactive quality support for global clinical trials, integrating Quality by Design and RBQM principles from protocol to submission. Requires 15-18 years in pharma/biotech, deep ICH GCP knowledge, and ex...

Lead global quality compliance audits for a leading biotech company in Hyderabad. This senior role requires 12-15 years of pharma/biotech quality/manufacturing experience and Lead Auditor certification. You will ensure regulatory compliance across sites and suppliers, with up to 50% travel. We of...