Process Engineer II

🏢 Genetixbiotherapeutics · 📍 Somerville, MA · 💼 hybrid 💰 $90,000 - $90,000 / yr
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Position Summary & Responsibilities

 

About Genetix Biotherapeutics

At Genetix Biotherapeutics every role has meaning, every team member is respected, and every day is a chance to make a difference. When you join Genetix, you're not just landing a new role, you become part of a company that's pursuing curative gene therapies to give patients and their families more days. We are doers, thinkers and collaborators who embrace and live by our values:

Our innovation is rooted in the diversity of our teams and results are achieved through cooperation and the integration of multiple viewpoints. This is personal and we approach every challenge with radical care.

This is a full-time hybrid position (3 days a week) in our Somerville – Assembly Row, Massachusetts office.

Role Summary:
As a Process Engineer II in the Manufacturing Sciences and Technology (MSAT) team at Genetix, you will play a pivotal role in ensuring the seamless technology transfer and technical support of our platform in cGMP manufacturing. This position focuses on supporting ongoing commercial production, execution of projects within the CMC lifecycle and tech transfer. You will collaborate closely with Technical Development, Quality, and our CDMO (Contract Development and Manufacturing Organization) partners to guarantee that all aspects of technology transfer and technical support are executed effectively.

Key Responsibilities:

  • Act as the primary technical expert for supporting the GMP production of autologous cell therapies at our CDMO partners.
  • Conduct complex manufacturing investigations using root cause analysis tools to determine underlying causes and develop corrective and preventive actions to prevent recurrence.
  • Develop and maintain process trending and continued process verification programs to ensure processes remain in a controlled state.
  • Drive a culture of continuous improvement and operational excellence through the identification and execution of key projects that enhance process performance.
  • Serve as a core team leader for cross-functional tech transfer teams, coordinating and tracking program progress within various workstreams.
  • Prepare and review technical documentation in
🎯 Candidate Preparation Guide For Genetixbiotherapeutics Applicants

Key Role Competencies & Evaluation Highlights

Key Role Focus:

Rigorous scientific precision, unwavering commitment to regulatory compliance, and translational drug development capability.

📋 Preparation Priorities (Key Areas to Clarify):
  • 1. Handwaving over critical experimental controls or reproducibility issues.
  • 2. Disregard for cross-functional bottlenecks between R&D and clinical teams.
  • 3. Overhyping early-stage pre-clinical results.
✨ Recommended Role Alignment Hook:

My background combines rigorous genomic science with a relentless focus on accelerating clinical translation safely.

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