Process Engineer: Tech Transfer Lead for Pharma/Biotech

Virtue America; Jacksonville (NC); On-site; USD 85,000 - 110,000; Full time

Job summary

Virtue America is seeking a Process Engineer with hands-on Technology Transfer experience to support a leading Pharmaceutical and Biotechnology project. The role involves leading Technology Transfer from development to manufacturing, transferring processes and knowledge between sites, and ensuring GMP/cGMP compliance to support scale-up and manufacturing readiness.

You will collaborate with Manufacturing, R&D, Quality, Validation, and Engineering teams, preparing documentation and driving

Qualifications

• Strong Process Engineering experience in Pharma, Biotech, or Life Sciences.
• Strong Technology Transfer experience is the primary requirement.
• Experience transferring processes from development to manufacturing or between manufacturing sites.
• Strong understanding of GMP/cGMP manufacturing environments.
• Excellent communication, problem-solving, and cross-functional collaboration skills.

Responsibilities

• Lead and support Technology Transfer activities from development/R&D to manufacturing.
• Transfer processes, procedures, and technical knowledge between development and manufacturing teams/sites.
• Support process scale-up, optimization, troubleshooting, and manufacturing readiness.
• Collaborate with Manufacturing, R&D, Quality, Validation, and Engineering teams.
• Prepare and review technology transfer documentation, process reports, SOPs, and manufacturing documentation.
• Support process troubleshooting and continuous improvement activities.
• Ensure processes comply with GMP/cGMP requirements.

Skills

Process Engineering

Technology Transfer

GMP/cGMP

Cross-functional Collaboration

Communication

Problem Solving

Job description

Virtue America is seeking a Process Engineer with hands-on Technology Transfer experience to support a leading Pharmaceutical and Biotechnology project. The role involves leading Technology Transfer from development to manufacturing, transferring processes and knowledge between sites, and ensuring GMP/cGMP compliance to support scale-up and manufacturing readiness.

You will collaborate with Manufacturing, R&D, Quality, Validation, and Engineering teams, preparing documentation and driving