Director, Biologics & CGT Operations

Frontage Laboratories

Exton (PA)

On-site

USD 180,000 - 270,000

Full time

14 days+
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Benefits offered by this job

Health insurance
Dental insurance
401(k) plan
Disability insurance
Life insurance

Job summary

Frontage Laboratories is seeking a Director of Biologics, Cell & Gene Therapy to lead technical operations, business growth, and service delivery for ATMP/CGT programs in a client-facing capacity. You will direct analytical development, process transfer, and regulatory readiness across viral vectors, cell therapies, and biologics.

The role requires a PhD or MS with 10+ years in biopharma and at least 4+ years in a leadership position within a CDMO/CRO, with a strong track record in client

Qualifications

  • PhD or MS in biotechnology, bioengineering, molecular biology, biochemistry, or related life sciences field.
  • 10+ years in biopharma with 4+ years in CDMO/CRO leadership.
  • Demonstrated client-facing leadership and multi-project portfolio management in ATMP/CGT.

Responsibilities

  • Lead high-visibility governance with external biopharma partners as executive contact for problem-solving and milestone delivery.
  • Scope technical proposals with BD teams, develop SOWs, assess technical feasibility and present capabilities in client meetings and facility audits.
  • Direct cross-functional teams through client tech transfers, analytical method development/validation, and cGMP testing for clinical/commercial products.
  • Ensure compliance with global cGMP/GLP regulations and host client audits and regulatory inspections.

Skills

Client-facing leadership
Technical breadth

Education

PhD or MS in biotechnology or life sciences

Job description

Frontage Laboratories is seeking a Director of Biologics, Cell & Gene Therapy to lead technical operations, business growth, and service delivery for ATMP/CGT programs in a client-facing capacity. You will direct analytical development, process transfer, and regulatory readiness across viral vectors, cell therapies, and biologics.

The role requires a PhD or MS with 10+ years in biopharma and at least 4+ years in a leadership position within a CDMO/CRO, with a strong track record in client

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