Project Manager - LNP at Genscript Biotech

Redmond, Washington, United States -

Full Time

Start Date

Immediate

Expiry Date

14 Jul, 26

Salary

85000.0

Posted On

15 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Lipid Nanoparticle Formulation, RNA Biology, Cross-functional Team Leadership, Scientific Troubleshooting, Client Relationship Management, Process Development, Data Analysis, Technical Documentation, Communication Skills, Problem-solving, Business Acumen, Bioinformatics, Laboratory Data Management, Time Management, Analytical Skills

Industry

Biotechnology Research

Description

About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. Role Description: We are seeking a dynamic Project Manager to lead customer-facing mRNA and lipid nanoparticle (LNP) projects, with a primary focus on LNP development and delivery. You will be responsible for ensuring all project deliverables are executed on time, within scope, and aligned with client expectations. The ideal candidate brings a solid scientific foundation, exceptional communication skills, sharp problem-solving abilities, and strong business acumen. You’ll serve as the key liaison between external clients and internal cross-functional teams — from R&D to manufacturing — requiring agility, diplomacy, and a results-driven mindset. Success in this role demands someone who thrives in GenScript’s fast-paced, collaborative, and high-performance culture. Key Responsibilities: Partner with Commercial and Production teams to ensure seamless project execution and customer satisfaction. Capture detailed project requirements, clarify specifications, and align expectations with clients. Develop and communicate customized project plans to clients and internal stakeholders. Monitor order production progress, evaluate performance metrics, and implement process improvements. Provide scientific troubleshooting for unexpected results and propose data-driven solutions. Deliver timely project updates to clients via email/telecom, adhering to agreed milestones. Lead cross-functional coordination across all project phases (initiation to closure). Address client complaints or quality concerns, collaborating with Production to resolve issues. Maintain comprehensive project documentation (reports, records, and compliance files). Support Production in analyzing and expanding service offerings for the US market. Serve as an R&D consultant, translating client needs into actionable research plans. Represent the company at customer visits and scientific events (conferences, workshops). Fulfill additional tasks assigned by Project Leaders, upholding service excellence. Qualifications: Master’s degree or higher in Chemical Engineering, Pharmaceutical Sciences, or a related field. Strong technical foundation in RNA biology and lipid nanoparticle (LNP) formulation, with hands-on laboratory or process development experience. Prior project management experience preferred — demonstrated success in coordinating cross-functional teams to deliver projects on time, within scope, and on budget. Direct research or development experience with mRNA and LNP platforms is a strong plus. Customer-centric mindset with excellent interpersonal and client-facing communication skills — both written and verbal. Proficient in Microsoft Office Suite and familiar with common bioinformatics or lab data management tools. Highly organized with strong analytical, prioritization, and time management skills. Proven ability to juggle multiple projects simultaneously without compromising quality or deadlines. Resilient under pressure — thrives in fast-paced, high-stakes environments. Benefit: Medical Insurance/ Vision Insurance/ Dental Insurance 401(k) & Retirement Savings Plan (RSP) Short Term Disability Insurance New Child Leave Paid Time Off Paid Company Holidays per year Paid Sick Days (earned based on hours worked) Compassionate Leave Jury Duty Leave Float day Personal days Perks: Free colleague meals during shift Onsite massages Charis Onsite gyms Compensation: Salary range: $70,000 – $85,000 total compensation, including bonus, depending on experience and qualifications. GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Responsibilities

The Project Manager will lead customer-facing mRNA and lipid nanoparticle projects by coordinating between R&D, manufacturing, and clients to ensure timely delivery. They are responsible for managing project plans, troubleshooting scientific issues, and maintaining comprehensive project documentation.