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Job description
Join Amgen's Mission of Serving Patients. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Facilitate real-time decision making to ensure adherence to GMP quality requirements. Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations.
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a person with strong cGMP and GDP behaviors, experience in biotechnology or pharmaceutical plant start up, and knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment.
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Healthcare
Amgen is a global biotechnology leader that develops biologic and human therapeutics to treat serious diseases such as cancer, heart disease, osteoporosis, inflammatory disorders, and rare conditions. Leveraging advanced genetic data and cutting-edge technology, the company maintains a robust R&D pipeline that expands its existing portfolio of life-changing medicines. Amgen’s commitment to innovation is reflected in its status as a Dow Jones Industrial Average constituent, a Nasdaq 100 member, and a Fast Company World's Most Innovative Companies honoree. The firm is recognized for its strong employee culture, earning a spot on Forbes’ list of America’s Best Large Employers. Amgen’s pioneering approach to drug discovery and development continues to set industry standards and improve patient outcomes worldwide.