Director, Biologics & CGT Operations

Frontage-Laboratories

Exton (PA)

On-site

USD 180,000 - 240,000

Full time

12 days ago
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Benefits offered by this job

Health and dental insurance
401(k) plan
Disability insurance
Life insurance

Job summary

Frontage Laboratories in Exton, PA, is seeking a Director of Biologics, Cell & Gene Therapy to lead technical operations, growth, and service delivery across viral vectors, cell therapies, and recombinant biologics.

The role requires 10+ years in biopharma, with 4+ in a CDMO/CRO leadership capacity, and strong client relationships, regulatory know-how, and strategic oversight to drive high-margin programs and global audits.

Qualifications

  • Education: Ph.D. or M.S. in Biotechnology, Bioengineering, Molecular Biology, Biochemistry, or related life sciences field.
  • Experience: 10+ years in biopharma with 4+ years in a leadership role within CDMO/CRO or contract testing.
  • Client-facing leadership: success managing client relationships, SOW scope, revenue targets, and multi-project portfolios in ATMP/CGT.
  • Technical breadth: deep knowledge of process/analytical development, vector biomanufacturing, cell processing, and regulatory expectations for ATMP/CGT services.

Responsibilities

  • Lead external biopharma partnerships as executive point of contact for governance and milestone delivery.
  • Collaborate with BD to scope technical proposals and develop SOWs, evaluating feasibility and presenting capabilities.
  • Direct cross-functional teams through technology transfers, analytics development/validation, and CGMP product testing.
  • Ensure global cGMP/GLP compliance and host client audits and regulatory inspections.

Skills

Client-facing leadership
Regulatory knowledge
Leadership experience
Biopharma industry experience

Education

Ph.D. or M.S. in Biotechnology/Biochemistry/Life Sciences

Job description

Frontage Laboratories in Exton, PA, is seeking a Director of Biologics, Cell & Gene Therapy to lead technical operations, growth, and service delivery across viral vectors, cell therapies, and recombinant biologics.

The role requires 10+ years in biopharma, with 4+ in a CDMO/CRO leadership capacity, and strong client relationships, regulatory know-how, and strategic oversight to drive high-margin programs and global audits.

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