MSAT Data Science Engineer

include, but are not limited to:

· Ownership of data lake infrastructure, including data ingestion, cleaning, organization, visualization and integration with data analysis tools.

· Translate process understanding into data and develop data analysis methodology to inform process and quality decisions.

· Generate data packages to support PPQ-readiness, PPQ execution and BLA submission for allogeneic CAR-T therapies and critical starting materials

· Able to apply and develop advanced technologies, scientific principles, theories and concepts to meet the needs of the Process Development and Manufacturing teams, including support of technology transfers

· In-depth knowledge of GMP and regulatory expectations and experience with regulatory inspections

· Work with Quality, Facilities & Engineering, Process Development and IT to ensure cross-functional alignment

· Closely partner with the Process Development and Quality groups to ensure continuity of data, robust process design and monitoring of product quality

· Contribute to company-wide AI initiatives as a thought leader for introduction and implementation of new AI tools for continuous improvement and innovation.

· Engage with broader manufacturing team to enable accomplishment of department goals

· Other duties as assigned

· Bachelor’s degree in science or engineering (with a focus on computer science or data science preferred) with a minimum of 6 years of experience within a GMP pharmaceutical manufacturing space and 2 years of direct data science experience within a GMP pharmaceutical manufacturing space.

· Late-stage clinical and commercial experience preferred.

· Proficiency in programming languages including SQL, Python and R and data analytics tools, including JMP, Spotfire, Tableau, R-Studio

· Knowledge of pharmaceutical manufacturing processes and GMP requirements for data integrity.

Cell therapy experience preferred.

· Experience developing and implementing data solutions with machine learning and AI preferred.

· Excellent written and verbal communication skills

· Excellent organizational skills and an ability to prioritize effectively to deliver results within established timelines

· Ability to work independently and as part of a team

· Ability to travel up to 10%

· Candidates must be authorized to work in the U.S.

We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more.

The expected salary range for this role is $120,000 to $140,00 per year.

Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.

As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought, designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.

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