Qualifications

• Ph.D. in Bioengineering, Chemical Engineering, Immunology or similar with 4+ years' technical experience or B.S./M.S. with 8+ years in cell therapy process development.
• Expertise in statistical experimental design (DOE) and proficiency in JMP software.
• Experience with authoring regulatory filings and supporting documents.
• Strong leadership skills for cross-functional teams and project management.
• Knowledge of immunology, cell biology, and analytical techniques such as flow cytometry and cell-based assays.
• Excellent technical writing and presentation skills.
• Willingness to work flexible hours, including occasional weekends.

Responsibilities

• Lead and mentor a team of associate scientists/engineers in process development activities.
• Design and analyze experiments focusing on cell processing methods' effects on T-cell biology.
• Collaborate with teams like MSAT and Analytical for material generation requests.
• Drive automation and optimization initiatives to enhance efficiency in processes.
• Author, review, and approve various regulatory documents and development reports.
• Participate in and potentially lead cross-functional projects or teams.
• Communicate research findings and ideas clearly to stakeholders both verbally and in writing.

Benefits

• Opportunity to lead a team and mentor upcoming scientists and engineers.
• Engagement in cross-functional collaboration, fostering diverse knowledge.
• Chance to work at the cutting edge of cell therapy development.
• Flexibility in work schedule, accommodating both regular and weekend hours.