Process Development Senior Scientist

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, happy lives. Our award‑winning culture is collaborative, innovative, and science‑based. If you have a passion for challenges and the opportunities that lie within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Process Development Senior Scientist What You Will Do Let’s do this. Let’s change the world. In this vital role you will join our Drug Substance Technologies – Synthetics (DSTS) group at either our Thousand Oaks, California or Cambridge, Massachusetts campus. In this dynamic role, you will drive innovative solutions to support manufacturing of therapeutic peptides at various stages of development; pre‑IND through commercial production. The successful candidate will have a strong background and experience in industrialization of solid‑phase peptide synthesis, ideally complemented with experience in peptide purification, isolation, and characterization techniques. You will be highly motivated, team‑oriented, and have a proven track record of scientific innovation and achievement. Responsibilities Work effectively with a diverse team of synthetic chemists, chemical engineers, and analytical chemists to develop scalable synthetic processes utilizing solid‑phase peptide synthesis. Drive technology innovation in solid‑phase synthesis, purification, and characterization of synthetic peptides. Support cGMP manufacturing and technology transfer to external contract manufacturers. Advance enabling technologies to accelerate pharmaceutical development and improve sustainability and process efficiency. Ensure process performance through process understanding, modeling, and characterization. Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc. Work cross‑functionally to deliver regulatory documents and support regulatory filings. Serve as a technical expert and keep current in the field of solid‑phase peptide synthesis. Work independently advancing projects and studies within required deadlines. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications. Basic Qualifications Doctorate degree: PhD, PharmD, or MD (with relevant post‑doc where applicable). Master’s degree and 3 years of scientific experience. Bachelor’s degree and 5 years of scientific experience. Preferred Qualifications Ph.D. in organic chemistry, biochemistry, or chemical engineering with expertise in synthetic peptide process development. Extensive hands‑on expertise in the synthesis and purification of synthetic peptides produced by solid‑phase synthesis. Experience within the pharmaceutical/biotech industry developing solid‑phase peptide synthesis processes and scaling/transferring the process into GMP manufacturing. Proficiency in analytical characterization techniques such as HIC‑HPLC, SEC, LC‑MS, IEX, and RP‑HPLC. Familiarity with laboratory automation, data analysis, and visualization techniques and tools. Track record of peer‑reviewed publications and research presentations. Demonstrated ability to work within a dynamic and interdisciplinary environment to achieve results. Excellent written and verbal communication skills, ability to multitask, effectively plan, and follow through on complex projects. A research summary included with CV is strongly encouraged. What you can expect of us As we work to develop treatments that take care of others, we also care for your professional and personal growth and well‑being. From our competitive benefits to our collaborative culture, we 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 consisting of: 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 flexible spending accounts. A discretionary annual bonus program, or for field sales representatives, a sales‑based incentive plan. Stock‑based long‑term incentives. Award‑winning time‑off plans. Flexible work models where possible (refer to the work location type in the job posting). Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. #J-18808-Ljbffr BioSpace