Quality Control Associate

Career Category Operations Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. 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. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Quality Control What you will do Let’s do this. Let’s change the world. In this vital role you will be responsible for activities including microbiology & analytical testing, sample and data management and equipment and instrumentation operation and maintenance in a highly dynamic, team environment. This role is expected to work a 10-hour shift Saturday - Tuesday, from 6:45AM-5:15PM. Responsibilities include: Responsible for one or more of the following activities in Quality Control including analytical testing, characterization, sample and data management Perform sample collection and sample handling to support GMP operations Perform testing and possible data review for compendia, non-compendia methods, and routine laboratory procedures Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks Operate and maintain specialized laboratory equipment and instrumentation Participate in laboratory investigations and audits as necessary Perform general laboratory housekeeping activities Maintain training compliance and proficiency At all times, comply with safety guidelines, cGMPs and other applicable regulatory requirements What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a good teammate with these qualifications.

High school/GED + 2 years [Job Code’s Discipline and/or Sub-Discipline] work experience OR​ Associate’s + 6 months [Job Code’s Discipline and/or Sub-Discipline] work experience OR​ Bachelor’s​ Preferred Qualifications: Experience in a regulated biotechnology/pharmaceutical lab environment Professional work experience in a fast-paced, flexible GxP Microbiology Laboratory Experience executing microbiological test methods (ie. Endotoxin, PCR, Growth Promotion Testing) Experience supporting Environmental and Clean Utility monitoring programs Demonstrated written and oral communication skills with ability to write effective science-based quality and compliance documents Demonstrated ability to be flexible and adaptable to support business needs Experience executing endotoxin, media qualification and sterility testing Demonstrated proficiency with electronic systems (LIMS, LMES, Trackwise, etc.) Exposure to Operational Excellence initiatives including Lean Manufacturing and 5S Demonstrated project management and presentation skills, and proven ability to manage priorities effectively What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. The expected