Develop a highly productive stable CHO cell line for cGMP biotherapeutic manufacturing.
Lead CLD work and contribute to cross-functional CMC timelines.
Hands-on work on new technology improvement projects and routine tasks.
Generate reliable data, author technical reports, and present findings to audiences.
Adhere to safety, GxP, and material handling standards.

🎯 Requirements

Bachelor’s Degree with 5+ years or Master’s Degree with 3+ years in relevant field.
Experience in mammalian cell culture and aseptic technique.
Strong attention to detail, time management, and multi-tasking.
Good verbal and written communication; collaborative mindset.

🎁 Benefits

Competitive compensation package (min to max listed).
Comprehensive benefits including PTO, health/dental/vision, 401(k).
Equity of equal opportunity in employment.

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