Quality Control Senior Associate

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-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. Senior Associate Quality Control What You Will Do Let's do this. Let's change the world! In this vital role, you will support: Sample Plan templating, logging and compilation of LIMS packets needed to support manufacturing Hosting and participating in cross-functional, cross-site, and external meetings to support internal and external testing. Management support of Contract Laboratory testing as required to support the manufacturing of Amgen products to ensure testing is completed on time per Quality Agreements and Disposition Due Dates. Support includes tracking of samples, data entry and issue resolution. Certificate of Analysis generation and Lot tracking for testing that supports disposition of product and raw materials Support Method Transfer and Validation activities in support of manufacturing timelines Document management What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. The professional we seek is an individual with the following qualifications: Basic Qualifications High school/GED + 4 years of Quality experience OR Associate's + 2 years of Quality experience OR Bachelor's degree and 6 months of Quality or Operations experience Master's degree Preferred Qualifications Professional work experience in a fast-paced, flexible GMP laboratory. Ability to generate and revise methods, reports and SOPs within CDOCs. Demonstrated proficiency with electronic systems (LIMS, LMES, CIMS, CDOCS, etc.). Ability to generate, update, triage, and close deviations and analytical test result assessments. Ability to manage and lead Operational Excellence initiatives including 5S and Standard Work associated with the testing labs. Demonstrated written and oral communication skills, project management and presentation skills, and proven ability to manage priorities effectively. Demonstrated ability to be flexible and adaptable to support business needs. 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 annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and #J-18808-Ljbffr