Process Engineer, Biotech Manufacturing & MS&T (Hybrid)

Taysha Gene Therapies; Baltimore (MD); On-site; 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

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