PackGene Japan Agent Recruitment Plan Is Officially Launched — Partner with a Global Leading CRO & CDMO to Shape the Future of Gene Therapy

  • PackGene Biotech is a world-leading CRO and CDMO, excelling in AAV vectors, mRNA, plasmid DNA, and lentiviral vector solutions. With profound technical expertise, exceptional operational capabilities, and high-quality project delivery, we offer global clients integrated CMC services spanning from early-stage concept validation and druggability assessment to IIT, IND, and BLA phases. We aim to accelerate the launch of innovative gene therapies and make them accessible to more people. Our comprehensive services include plasmid, viral vector, and mRNA manufacturing, supporting full-spectrum needs from R&D to commercialization.

Ideal Partner

We cordially invite qualified enterprises in Japan to become our regional partners. Ideal candidates should meet the following criteria:

  • Location: Nationwide coverage in Japan, with priority given to biopharma hub cities such as Tokyo, Osaka, Kyoto, and Sapporo.
  • Industry Experience: Possess sales channels and market resources in related fields such as biopharmaceuticals, life science reagents, lab equipment, and CRO/CDMO services.
  • Customer Base: Familiar with and currently serving clients including innovative pharmaceutical companies, research institutes, university laboratories, and hospital R&D departments.
  • Team Capability: Equipped with a professional technical sales team capable of conducting online and offline promotion activities independently.

Why Partner with PackGene?  

  • Extensive Project Experience: 50,000+ AAV delivered, scalable to GMP grade, 200+Batches of pilot scale AAV , serving 2,100+ Academia, biotech & big pharma globally and 50+ MNC.
  • State-of-the-Art Facilities: One-stop service from vector design to IND/BLA, High-yield, robust,and scalable production platform for AAV、 plasmid 、mRNA、LV.
  • Stringent Quality Standards: AAV reference standard and AAV analytical method transferred to NIFDC, FDA/NMPA IND approval without supplement.
  • Efficient Project Turnaround: Streamlined processes enable industry-leading delivery speed.

Support for Our Partners

  • Professional Training

    Comprehensive technical materials and expert-led training with ongoing English technical support.
  • Marketing Support

    Full suite of promotional materials and co-developed strategies tailored to regional needs.
  • Business Benefits

    Tiered commission structure and annual performance incentives-specific terms available upon consultation.

Application Process

1.  Submit Application: Email company profile, business overview, and sales team introduction to bd@packgene.com.
2.  Initial Review:Application materials will be reviewed within 5 business days, followed by an online meeting.
3.  Due Diligence: On-site visits may be conducted to confirm mutual fit and resource alignment.
4.  Contract Signing: Negotiation of agent regions, sales targets, and support terms before formal agreement.
5.  Launch Collaboration:Commence market promotion and customer services after training completion.

Contact US

Interested companies are welcome to reach out via bd@packgene.com or fill out the form below. Let’s collaborate to create a new future in gene therapy together!

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