Process Engineer, Biotech MS&T - Remote/Travel

Taysha Gene Therapies; United States; Remote; USD 95,000 - 105,000; Full time

Benefits offered by this job

Stock options

ESPP program

Performance bonus

401(k) with matching

Medical/dental/vision benefits

Generous vacation/holiday schedule

Job summary

Taysha Gene Therapies is seeking a Process Engineer, Manufacturing and MS&T to advance manufacturing process development for AAV gene therapy products. You will oversee tech transfers, CAPAs, and change controls at the CDMO, ensuring quality and regulatory compliance across clinical and commercial supply.

The role requires a Bachelor's in science or engineering, 1–5 years of biotech manufacturing experience, and strong project management with travel up to 25%.

Qualifications

• Bachelor's degree in science or engineering.
• 1–5 years' experience in biotech/pharma manufacturing with cGMP exposure.
• Knowledge of high-purity AAV gene therapy manufacturing processes preferred.
• Strong project management and time-management skills.
• Excellent written and verbal communication skills.
• Willingness to travel up to 25%.

Responsibilities

• Oversee investigation and resolution of manufacturing issues.
• Collaborate with CDMO to ensure compliant lifecycle activities.
• Prepare risk assessments, process descriptions, and transfer docs.
• Review and approve CDMO PFDs, MPRs, SOPs, and Reports.
• Provide on-site plant support during manufacturing at CDMO.
• Support process development activities and drive improvements.
• Contribute to SOPs and cross-functional goals.
• Support QA audits and regulatory inspections.

Skills

Project management

Communication skills

Time management

Leadership

Education

Bachelor's degree in science or engineering

Job description

Taysha Gene Therapies is seeking a Process Engineer, Manufacturing and MS&T to advance manufacturing process development for AAV gene therapy products. You will oversee tech transfers, CAPAs, and change controls at the CDMO, ensuring quality and regulatory compliance across clinical and commercial supply.

The role requires a Bachelor's in science or engineering, 1–5 years of biotech manufacturing experience, and strong project management with travel up to 25%.