Process Engineer, Manufacturing and MS&T

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

Overview of Position
The Process Engineer, Manufacturing and MS&T, is responsible for contributing to the development, optimization and continuous improvement of manufacturing processes. This role ensures the successful and compliant production of high quality AAV-based gene therapy products by providing scientific and technical expertise throughout the product lifecycle, from process scale-up and technology transfer to commercial manufacturing support and troubleshooting. This position will provide oversight of manufacturing activities at Taysha's selected CDMO for investigational and commercial drug substance and drug product to ensure products and intermediates are delivered to meet Taysha's product specifications, quality, regulatory and timeline requirements.

The preferred location is either Morrisville, NC site (with regular travel to our CDMO partner site) or remotely based in Baltimore, MD.

Essential Duties

• Oversee investigation, evaluation and resolution of manufacturing issues, including evaluation of deviations, technical changes and CAPAs to materials, manufacturing processes and product specifications.
• Liaise and collaborate with Taysha and CDMO functional groups to ensure compliant management of product lifecycle activities including PPQs, comparability, CPV, change controls, tech transfers (development to manufacturing, site-to-site), etc.
• Author/review/approve risk assessments, process descriptions, control strategies, tech transfer documentation, regulatory submission documentation and other related MS&T documentation required for manufacture of process intermediates, drug substance and drug product.
• Review/approve CDMO PFDs, MPRs, SOPs, Sample Plans, Assessments, Protocols and Reports in support of clinical and commercial supply manufacturing.
• Provide in-person plant support during manufacturing at CDMO.
• Provide Manufacturing/MS&T technical support to process development activities as required.
• Identify and implement process monitoring and control strategies to ensure manufacturing consistency and drive improvements in efficiency and quality.
• Contribute to the development and improvement of department-level and cross-functional goals and objectives, Standard Operating Procedures (SOPs), business processes, systems, and tools.
• Support and participate in Quality Assurance audits and regulatory inspections.

Skill & Education Requirements

• Bachelor's Degree in science or engineering required.
• 1-5 years' experience in the biotechnology or pharmaceutical manufacturing industry with direct experience in cGMP manufacturing or manufacturing sciences.
• Knowledge of high-purity suspension-based AAV gene therapy manufacturing process operations preferred.
• Demonstrated ability to manage complex projects and competing priorities.
• Excellent written and oral communication skills.
• A proven self-starter with excellent time management skills.
• Ability to travel up to 25% at times.

Base compensation range at time of posting: $95,000 - 105,000. The actual base salary depends, in part, on the successful candidate’s qualifications for the role, including education and experience.

Taysha offers a comprehensive compensation and benefits program to eligible employees, including:

• Individual Stock Option awards
• ESPP program
• eligibility to participate in performance bonus program
• company-sponsored 401(k) with matching contribution
• eligibility for medical, dental, vision and prescription drug benefits
• a generous vacation/holiday schedule

Note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Taysha is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Taysha are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.