MSAT Process Engineer II – Gene Therapy Scale-Up

AskBio Inc.; Durham (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

AskBio Inc. seeks a Process Engineer II to join the MSAT Process Engineering team at the RTP HQ in North Carolina.

The role supports scale-up, technology transfer of gene therapy programs into cGMP manufacturing for clinical production and commercial launch, with involvement in PPQ readiness and Phase III activities. You will collaborate across functions, develop small-scale models, document protocols, and help ensure continuity of supply while meeting global regulations.

Qualifications

• Bachelor’s Degree in a scientific discipline with 2+ years of biopharmaceutical experience, or a Master’s Degree.
• High School Diploma with 6+ years biopharmaceutical experience.

Responsibilities

• Collaborate with cross-functional teams to transfer small-scale gene therapy processes to the MSAT lab and scale up.
• Perform process characterization experiments to define the PPQ process control strategy.
• Develop and qualify small-scale models predictive of the cGMP scale.
• Author protocols and reports; maintain electronic laboratory notebooks.
• Provide effective communication of experimental results to internal stakeholders.
• Support investigations with data-driven root-cause analyses.
• Ensure the laboratory is clean, organized and maintained; schedule routine maintenance and equipment calibration.

Skills

Biomanufacturing experience

Communication skills

Microsoft Office

Team collaboration

Problem solving

Willing to travel

DOE methodology

Education

Bachelor’s Degree in a scientific discipline

Master’s Degree in a scientific discipline

High School Diploma with 6+ years biopharmaceutical experience

Tools

JMP

Job description

AskBio Inc. seeks a Process Engineer II to join the MSAT Process Engineering team at the RTP HQ in North Carolina.

The role supports scale-up, technology transfer of gene therapy programs into cGMP manufacturing for clinical production and commercial launch, with involvement in PPQ readiness and Phase III activities. You will collaborate across functions, develop small-scale models, document protocols, and help ensure continuity of supply while meeting global regulations.