Project Manager

AGC Biologics•Bothell, WA

14d•$94,000 - $129,250

About The Position

AGC Biologics is seeking a Project Manager to lead biologics programs throughout the product lifecycle, from technology transfer and process development through GMP manufacturing. The role is accountable for delivering programs on time, within scope, and within budget while meeting client expectations and regulatory requirements. The Project Manager works within the Program Management team and coordinates activities across Process Development, Manufacturing, Quality, MSAT, Analytical, Regulatory, and Supply Chain functions, while supporting strong client relationships and business growth. The position leads CMC development, technology transfer, and GMP manufacturing programs from initiation through close-out; develops project plans; manages risks, issues, project financials, and contractual commitments; and provides milestone updates and forecasts. It also supports late-stage activities such as PPQ readiness, regulatory submissions, and commercialization. The role is located in Bothell, Washington, and is full-time. Compensation is $94,000–$129,250, based on experience.

Requirements

Bachelor’s degree in Life Sciences, Chemistry, Biotechnology, Engineering, or a related field.
3–8 years of experience within biopharmaceutical, biotechnology, or CDMO environments.
2–5 years of direct project management experience.
Strong knowledge of GMP regulations and regulated manufacturing environments.
Experience with project management tools such as PPM systems or Smartsheet.
Strong written and verbal communication skills, including the ability to engage senior stakeholders and clients.
Ability to lead and influence cross-functional teams without direct authority.
Strong problem-solving, decision-making, and conflict resolution skills.
Financial acumen, including experience managing budgets, contracts, and invoicing processes.
Strong planning, organization, and project execution capabilities.

Nice To Haves

2+ years of CDMO experience.
Experience supporting late-stage programs, including PPQ, BLA preparation, and commercialization activities.
Experience leading technology transfers and new product introductions.
Familiarity with TrackWise.

Responsibilities

Lead CMC development, technology transfer, and GMP manufacturing programs from project initiation through close-out.
Develop and maintain project plans to ensure delivery within scope, timeline, and budget.
Serve as the primary client point of contact, providing clear communication and program leadership.
Partner with Business Development to strengthen client relationships and support program growth.
Identify project risks, develop mitigation strategies, and facilitate issue resolution with functional leaders.
Establish contingency plans and escalate critical issues as needed.
Drive alignment across Process Development, Analytical, QC, QA, MSAT, Supply Chain, and Manufacturing teams.
Support late-stage activities, including PPQ readiness, regulatory submissions, and commercialization efforts.
Apply technical understanding of biologics development and manufacturing to support decision-making and technology transfer activities.
Manage project financials and contractual commitments, including Project Change Orders.
Provide milestone updates and forecasting information to support financial planning and client invoicing.