Business Development Manager, GMP Gene Editing & Biologics Manufacturing
Quick Summary
Sales & Revenue Growth Identify, prospect, and close new business for GMP gene-editing reagents and GMP peptide/protein manufacturing services.
Education & Experience Bachelor’s degree in Biology, Biochemistry, Molecular Biology, Biotechnology, or related field required; Master’s or MBA preferred.
The Business Development Manager will drive revenue growth across GenScript’s GMP Gene Editing and GMP Biologics Manufacturing portfolios. This individual will support sales of GMP-grade nucleic acid reagents (including guide RNAs, ssODNs, long ssDNA, dsDNA HDR templates, and custom endonucleases) as well as GMP peptide and recombinant protein manufacturing services supporting vaccines, protein therapeutics, and advanced cell and gene therapy programs.
This role requires strong technical fluency in gene editing or biologics development, outstanding consultative selling skills, and the ability to collaborate cross-functionally to deliver world-class customer experience.
This position can be based remotely in the United States but requires at least 25% travel. The estimated salary range is $100,000 - $135,000, based on experience level.
Responsibilities
~1 min read- Identify, prospect, and close new business for GMP gene-editing reagents and GMP peptide/protein manufacturing services.
- Develop and execute a territory sales plan to meet or exceed monthly, quarterly, and annual revenue targets.
- Manage the full sales lifecycle, including lead generation, discovery, scoping, proposal creation, negotiation, and closing.
- Build strong relationships with customers in cell therapy, gene therapy, vaccine development, and biologics R&D.
- Maintain pipeline visibility and forecasting accuracy using CRM systems (Salesforce, Dynamics).
- Serve as a technical resource for GMP manufacturing capabilities spanning: sgRNA, pegRNA, and custom guide RNA, ssODNs and long ssDNA, Linear dsDNA HDR donors (covalently closed), Custom endonucleases and engineered proteins, GMP peptides and recombinant proteins
- Translate complex scientific concepts into clear value propositions for R&D, technical, and CMC stakeholders.
- Support feasibility assessments and proposal development in collaboration with internal teams.
- Partner with Marketing, Project Management, Manufacturing, Quality, and R&D to ensure seamless customer onboarding and project execution.
- Communicate customer needs, trends, and feedback internally to refine service offerings and operational capabilities.
- Contribute to the development of sales enablement materials, technical content, and commercial positioning across the gene editing and biologics portfolio.
- Attend conferences, trade shows, and on-site customer meetings (25% or more travel).
- Expand GenScript’s presence through networking with KOLs, biotech leaders, and strategic partners.
- Monitor industry trends across gene editing, iPSC engineering, viral vector/mRNA workflows, and peptide/protein therapeutics
Requirements
~1 min read- Bachelor’s degree in Biology, Biochemistry, Molecular Biology, Biotechnology, or related field required; Master’s or MBA preferred.
- 3+ years of business development or sales experience in CDMO/CRO services within gene editing, biologics manufacturing, or adjacent markets.
- Demonstrated success in consultative technical selling and achieving revenue targets.
- Familiarity with GMP operations, CMC documentation, and regulatory expectations for nucleic acids, peptides, or recombinant proteins.
- Strong understanding of CRISPR workflows, HDR template design, and/or biologics development.
- Excellent relationship-building, communication, and negotiation skills.
- Ability to independently manage a dynamic pipeline within a fast-paced environment.
- Proficiency with Microsoft Office, Salesforce/Dynamics, and virtual communication platforms.
- Highly motivated, organized, detail-oriented, and capable of leading scientific and commercial discussions.
#LI-EB1
#GS
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.
Location & Eligibility
Listing Details
- Posted
- May 11, 2026
- First seen
- May 11, 2026
- Last seen
- May 11, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 67%
- Scored at
- May 11, 2026
Signal breakdown
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