Senior Manager Drug Substance Technology & Engineering

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, and 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 Manager Drug Substance Technology & Engineering What You Will Do Amgen is seeking a Senior Manager to join the Drug Substance Technology & Engineering (DSTE) team at our Thousand Oaks, California site. In this onsite leadership role, you will oversee downstream purification manufacturing support unit operations supporting both clinical and commercial biologics drug substance. You will lead a team of downstream process engineers and play a key role in early phase technology transfer and the manufacturing execution, process optimization, and strategic improvement initiatives across all phases of development and the commercialization lifecycle. This is an exciting opportunity for a strong technical and people leader who thrives in a highly collaborative, fast‑paced, and innovation‑driven environment. In addition to supporting commercial and pipeline programs, you will help shape cross‑functional initiatives that advance technology, process performance, and business outcomes. Location: Thousand Oaks, CA Travel: Up to 10% domestic and international travel Key Responsibilities Support the development, scale‑up, tech transfer and manufacturing execution of cGMP clinical and commercial downstream purification processes including, but not limited to, harvest, clarification, chromatography (Protein A, AEX, CEX, etc.), viral filtration, UF/DF, and sterile filtration. Apply engineering principles and statistical analysis in order to: Identify, develop and implement downstream process improvements into the manufacturing facility. Resolve technical issues observed during scale‑up and/or manufacturing execution of purification processes. Manage escalation and on‑floor support as required to achieve successful scale‑up and manufacturing objectives. Interface with process development teams to ensure processes are robust and are designed to deliver all quality attributes and enable manufacturing success. Collaborate with Process Development, Quality, Manufacturing, Regulatory, Validation and Supply Chain to drive continuous improvements into our business processes. Lead site activities for continuous process verification, process monitoring, optimization, complex investigation, and product life‑cycle management. Ensure safety and compliance of process development activities. Collaborate with other site‑functions and network drug substance teams in delivering plant goals. Lead cross‑functional teams to resolve complex problems while meeting quality, schedule, and cost objectives. Ensure manufacturing operations are aligned with the registered process. Provide support for regulatory filing, inspection, and other CMC activities. Serve as member of the ATO DSTE leadership team utilizing network thinking and innovative approaches to advance the drug substance organizational capabilities. Supervising Others / Team Experience Create multi‑year technical strategies for advancing business performance. Ensure that safe practices are followed. Provide mentoring and expertise to staff on the downstream team. Motivate, develop, and coach staff while promoting team collaboration. Apply effective management practices in the direction and development of others. Leadership and Influence Identify and negotiate resources and develop timelines for project activities. Collaborate within the department and interdepartmentally. Provide scientific and technical leadership. Ensure department staff are adequately developed and trained. Provide adequate feedback through coaching and effective performance appraisal and development planning. Initiate and encourage scientific collaboration with groups outside the department. Manage project resources (material, labor, time, etc.), and elevate relevant issues to project lead and line‑management. Build and maintain effective collaborations with partner organizations. Decision Making and Judgment Anticipate, proactively detect, and address problems related to departmental and interdepartmental activities. Inform and consult department head and senior staff appropriately. What We Expect Of You The dynamic individual we seek is a collaborative partner with these qualifications. Basic Qualifications Doctorate degree and 2 years of biologics process development or commercial‑scale technical support experience, or Masters degree and 6 years of biologics process development or commercial‑scale technical support experience, or Bachelors degree and 8 years of biologics process development or commercial‑scale technical support experience, or Associates degree and 10 years of biologics process development or commercial‑scale technical support experience, or High school diploma / GED and 12 years of biologics process development or commercial‑scale technical support experience. In addition to meeting at least one of the above requirements, you must have a minimum of 2 years of experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced above. Preferred Qualifications 8+ years of experience in a technical role supporting biotechnology processes within regulated environments (i.e., cGMP). 5+ years directly managing people and/or leadership experience leading teams, projects, and programs or directing the allocation of resources. Strong and in‑depth expertise in purification processes. Experience in process scale‑up, technology transfer, process validation, troubleshooting, and complex investigation. Strong oral and verbal communication skills, interact effectively with diverse internal and external stakeholders. Experience developing staff to reach their full potential. Knowledgeable in regulatory filings and inspections. Familiarity in operational aspects of commercial biopharma manufacturing. Familiarity in statistical analysis, analytical methods, and product quality attributes relevant to biological processing. What You Can Expect Of Us From our competitive benefits to our collaborative culture, we support your professional and personal growth and well‑being. 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: 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 to see if this applies. Apply now and make a lasting impact with the Amgen team. careers.amgen.com In any materials you submit, you may redact or remove age‑identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Sponsorship Sponsorship for this role is not guaranteed. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Equal Opportunity Employer 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