Bioconjugation Development Director & Tech Lead

Abzena Inc.

Bristol Township (Bucks County)

On-site

USD 170,000 - 210,000

Full time

14 days+
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Job summary

Abzena is seeking an Associate Director Bioconjugation Development to lead bioconjugation discovery and development activities at Abzena Bristol. You will oversee conjugation development, downstream purification, and scale-up to support client and internal programs.

The role involves mentoring staff, leading client meetings, contributing to proposals, and ensuring cGMP compliance while advancing technology through transfer to manufacturing teams.

Qualifications

  • PhD or MS/BS in biochemical sciences or bio-engineering with industry experience in biotherapeutic development or bioconjugation.
  • Experience in preparative purification of biological molecules.
  • Knowledge of chromatography systems and tangential flow filtration (TFF).

Responsibilities

  • Oversee Bioconjugation Development department operations and resource planning to deliver client and company projects.
  • Hands-on execution of chromatographic purifications, membrane filtrations, and conjugation work-up.
  • Perform and optimize bioanalytical characterization of bioconjugate products.
  • Project planning and management
  • Serve as bioconjugation technical lead for internal and external communications.
  • Mentorship, training and management of assigned reports.
  • Coordinate with QA/QC and Management for tox and GLP batch development.

Skills

Bioconjugation development
Team leadership
Client-facing communication
Project planning

Education

PhD or MS/BS in biochemical sciences or bio-engineering

Tools

AKTA systems
HPLC/LC-MS
TFF systems

Job description

Abzena is seeking an Associate Director Bioconjugation Development to lead bioconjugation discovery and development activities at Abzena Bristol. You will oversee conjugation development, downstream purification, and scale-up to support client and internal programs.

The role involves mentoring staff, leading client meetings, contributing to proposals, and ensuring cGMP compliance while advancing technology through transfer to manufacturing teams.

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