Process Engineer, Manufacturing and MS&T

Taysha Gene Therapies; Baltimore (MD); Remote; USD 95,000 - 105,000; Full time

Benefits offered by this job

Stock options

ESPP program

401(k) with matching

Medical, dental, vision benefits

Generous vacation/holiday schedule

Job summary

Taysha Gene Therapies seeks a Process Engineer, Manufacturing and MS&T to advance, optimize and scale AAV-based gene therapy manufacturing processes. You will work across tech transfer, process development and commercial support, collaborating with a CDMO to ensure product quality, compliance and on-time delivery.

The role offers remote-based work from Baltimore, MD, with occasional travel and a strong benefits package including stock options, ESPP, 401(k) matching, and medical/dental/vision

Qualifications

• 1-5 years’ experience in biotech/pharma manufacturing with cGMP exposure.
• Knowledge of high-purity suspension-based AAV manufacturing preferred.
• Demonstrated ability to manage complex projects and priorities.
• Excellent written and oral communication skills.
• Willingness to travel up to 25%.

Responsibilities

• Oversee investigation and resolution of manufacturing issues, CAPAs, deviations.
• Collaborate with CDMO and internal teams on lifecycle activities and tech transfers.
• Author/reg-review risk assessments, process descriptions, control strategies, docs.
• Review CDMO PFDs, MPRs, SOPs and regulatory submissions for clinical/commercial supply.
• Provide on-site manufacturing support at CDMO and MS&T technical guidance.
• Develop and implement process monitoring to improve efficiency and quality.
• Contribute to SOPs, business processes and cross-functional goals.
• Support QA audits and regulatory inspections.

Skills

Strong project management

Excellent communication

Self-starter with time management

Collaboration with CDMO

Ability to travel up to 25%

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. Th 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 and 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.