Director, Drug Product Manufacturing

Corbus Pharmaceuticals; Norwood (MA); On-site; USD 250,000 - 360,000; Full time

Job summary

Scorpion Therapeutics seeks a senior manufacturing leader to drive lead drug product manufacturing for both clinical and commercial programs. You will oversee external CMO/CDMO partnerships, technology transfer, and process validation, ensuring manufacturing readiness and cGMP compliance.

The role requires a PhD in a related field and 15+ years in pharma/biotech manufacturing, with strong outsourcing and regulatory experience. Hybrid work setup in Norwood, MA is offered.

Qualifications

• 15+ years in pharma/biotech manufacturing.
• Extensive experience managing outsourced production.
• Experience with process validation and regulatory support.
• Strong knowledge of cGMP and supply chain management.

Responsibilities

• Develop manufacturing strategies across clinical and commercial programs.
• Manage performance and ensure integration with supply chain.
• Support regulatory submissions and maintain cGMP compliance.
• Lead risk mitigation and facilitate cross-functional collaboration.

Skills

Leadership

Strategic planning

Cross-functional collaboration

Regulatory support

cGMP knowledge

Supply chain management

Education

PhD in Chemical Engineering

PhD in Pharmaceutical Sciences

PhD in Chemistry

PhD in Biochemistry

Related field

Job description

Role

Lead drug product manufacturing for clinical and commercial biopharmaceutical programs, overseeing external CMO/CDMO partnerships, technology transfer, process validation, and manufacturing readiness.

Responsibilities

develop manufacturing strategies, manage performance, ensure integration with supply chain, support regulatory submissions, and maintain cGMP compliance; lead risk mitigation and facilitate cross-functional collaboration.

Requirements

PhD in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or related; 15+ years in pharma/biotech manufacturing, with extensive experience managing outsourced production, process validation, and regulatory support; strong knowledge of cGMP and supply chain management.

HighValue

biologics and small molecules experience preferred; involvement in NDA/BLA/MAA processes; expertise supporting late-stage development, regulatory approvals, and commercial launch; experience in oncology and metabolic diseases advantageous.

WorkSetup

hybrid in Norwood, Massachusetts.