AGC Biologics

Compensation

Full Description

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. Job Summary We are looking for a Project Manager to lead biologics programs from technical transfer and process development through GMP manufacturing. In this role, you will oversee the full project lifecycle to ensure programs are delivered on time, within budget, and in compliance with regulatory requirements. The Project Manager serves as the primary liaison between clients and internal cross-functional teams, driving alignment across Process Development, Manufacturing, Quality, Regulatory, MSAT, and Supply Chain. This role is accountable for timelines, financial oversight, risk management, and clear communication throughout the program lifecycle. Your Key Responsibilities Lead CMC development, technology transfer, and GMP manufacturing programs from project award through closeout. Develop and maintain project plans, ensuring delivery within scope, timeline, and budget. Serve as the primary point of contact for clients, ensuring clear communication and expectation management. Partner with Business Development to support strong client relationships and program continuity. Identify and manage program risks, develop mitigation strategies, and escalate issues as needed. Drive alignment across cross-functional teams including PD, Analytical, QC, QA, MSAT, Supply Chain, and Manufacturing. Support late-stage program activities such as PPQ readiness, regulatory submissions (e.g., BLA), and commercialization planning. Apply knowledge of biologics development (cell line development, upstream/downstream processing, analytical requirements) to support technical discussions and decision-making. Manage financial and contractual elements of programs, including change orders and milestone tracking. Provide accurate financial updates to support forecasting and client invoicing. Key Skills Strong written and verbal communication skills for stakeholder and client management. Ability to lead cross-functional teams without direct authority. Effective problem-solving and conflict resolution skills. Solid financial acumen with understanding of contracts and invoicing processes. Qualifications Required Bachelor’s degree in Life Sciences, Chemistry, Biotechnology, Engineering, or related field. 3–8 years of experience in biopharmaceutical, biotech, or CDMO environments. 2–5 years of direct project management experience. Strong understanding of GMP environments and regulatory expectations. Experience using project management tools (e.g., PPM systems, Smartsheet). Preferred CDMO experience. Experience managing late-stage programs (PPQ, BLA preparation, commercialization readiness) and/or commercial programs. Experience leading technology transfer or new product introductions. Familiarity with TrackWise. Location: Bothell, WA Schedule: Full-time, onsite Compensation: $94,000 - $129,250 Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook! AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. AGC Biologics is Your Friendly CDMO Expert – dedicated partners with the expertise and commitment to support our customers and teams. We work with some of the world’s most innovative pharmaceutical companies to develop and manufacture their life-changing drug products. If you’re motivated by meaningful impact and ready to join our journey, we invite you to explore our current opportunities!