Post Doctoral Fellow

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. Post Doctoral Fellow What you will do Let’s do this. Let’s change the world. In this vital role Amgen is seeking a highly motivated Process Development Postdoctoral Fellow to join the Drug Product Technologies organization. The Fellow will lead an innovative research project focused on enabling high concentration biologic drug products through particle engineering and suspension based formulation and fill/finish approaches. The Drug Product Technologies group is responsible for phase appropriate drug product formulation and fill/finish process development for large molecule modalities (e.g. monoclonal antibodies, bispecific T-cell engagers (BiTEs), antibody drug conjugates (ADC’s) and fusion proteins).  Design and execute studies to develop high concentration protein formulations by evaluating viscosity reducing excipients and formulation strategies to enhance product performance and delivery   Participate in the execution and documentation of laboratory studies with a high degree of accuracy (e.g. UF/DF, spray drying, mixing, stability)  Evaluate product and process performance through analytical testing (e.g. SEC, CEX-U/HPLC, particle analysis, moisture content)  Apply solid-state (SEM, DSC, DVS) methods to establish relationships among formulation composition, particle structure, stability, and product performance   Perform rheological characterization of high concentration formulations and suspensions  Develop and evaluate concentrated protein suspension formulations for parenteral delivery, including assessment of device compatibility  Build a wide range of data and analytics solutions, from available commercial dashboarding tools such as TIBCO Spotfire, MS Smartsheet   Perform data analysis using statistical analysis software (e.g. JMP, SAS, etc.)  Author/review/data verify technical protocols and reports.  Participate in team meetings by sharing study results and technical challenges.  Adapt to flexible working hours to accommodate project needs and team collaboration.  Navigate and thrive in an environment with ambiguity, demonstrating adaptability and problem-solving skills.  Work effectively across different time zones and be respectful of diverse cultures.  What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.

PhD at time of appointment Preferred Qualifications: Familiarity with pharmaceutical/biotechnology process development  Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and align with company policies  Knowledge of Drug Product unit operations (i.e. ultrafiltration/diafiltration, filling, filtration,