Senior Data Quality Engineer (I, II, III)

Sorry, this job was removed at 10:08 a.m. (CST) on Thursday, Feb 26, 2026
South San Francisco, CA, USA
In-Office
90K-210K Annually
Biotech
The Role
Cellares is seeking an innovative and highly motivated Senior Data Quality Engineer who will contribute to the development of our advanced cell therapy manufacturing platform.

The primary focus of this position is to ensure the accuracy, reliability, and integrity of data within our data platform. The individual will participate on a cross-functional team, design, build, and maintain automated testing frameworks to ensure data integrity at every stage of our data pipelines. The successful candidate should have extensive experience in quality assurance for data platforms, ideally with significant hands-on experience in the Databricks environment. They should be detail-oriented and possess strong analytical and problem-solving skills.

Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. Candidates should be great team players with the ability to work with minimal supervision.

Responsibilities

  • Build and maintain automated data validation tests using Databricks notebooks and tools like Pytest
  • Test data ingestion, transformation, and loading processes within the Databricks Lakehouse, specifically focusing on the Bronze, Silver, and Gold layers of the Medallion architecture
  • Implement tests for data accuracy, completeness, consistency, timeliness, and uniqueness at different points in the pipeline to catch data issues early
  • Reconcile data by comparing record counts, schemas, and values between source systems and target tables in Databricks
  • Implement automated data quality checks within data pipelines to ensure no data regressions occur with new code deployments
  • Implement automated monitoring and alerting for data quality metrics, identifying anomalies in data freshness, schema evolution, and volume
  • Work closely with data engineers and product owners to understand data requirements and ensure data quality meets business needs
  • Ensure compliance with data governance policies by building quality checks that validate data sensitivity, masking, and lineage, leveraging tools like Unity Catalog
  • Communicate project status and new discoveries in a clear and timely manner during daily stand-ups

Requirements

  • Bachelor’s or Master’s in Computer Science, Electrical Engineering, or related field and 5+ years of relevant experience
  • Experience with data pipeline and data quality testing strategy and execution, with significant hands-on experience in the Databricks environment
  • Strong proficiency in Python for developing and executing data validation scripts
  • In-depth knowledge of Databricks, Delta Lake, and the Lakehouse architecture
  • Proficiency in writing complex SQL queries for data validation, reconciliation, and troubleshooting issues
  • Solid understanding of data warehousing concepts, including dimensional modeling (star/snowflake schemas)
  • Hands-on experience with Azure, including Azure storage and data services that integrate with Databricks
  • Ability to process data, interpret testing results and provide feedback to the team
  • Desire to be part of a rapidly evolving organization, with compelling technology, and taking products and processes to the next level
  • Self-awareness, integrity, authenticity, and a growth/entrepreneurial mindset

This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

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The Company
HQ: South San Francisco, CA
109 Employees
Year Founded: 2019

What We Do

Cellares is revolutionizing cell therapy manufacturing. We are developing a one-of-a-kind solution, The Cell Shuttle, to overcome the challenges associated with manufacturing so these life-saving therapies are affordable and widely available to patients who can benefit. The clinical impact of cell therapy in treating cancer has been proven, but this therapeutic approach has several limitations, especially in manufacturing, leaving extremely sick patients waiting for treatment and desperate for hope. Since cell therapy is currently produced for a single patient at a time, it is expensive to manufacture, requiring significant time and resources, and is difficult to scale. Preclinical and clinical scientists, as well as commercial cell therapy manufacturers also lack the options to fully automate their manufacturing process quickly, safely, cost-effectively and at the scale they need. The Cell Shuttle is an automated and closed end-to-end manufacturing solution that is flexible and scalable, enabling customers to run exact processes specified for their cell therapy. Compared with the current manual manufacturing processes for cell therapy, the Cell Shuttle’s next-generation automated manufacturing solution has 10 times the scalability (meaning 10 times more patient doses can be produced simultaneously), enables a three-fold reduction in process failure rates and will reduce the per-patient manufacturing cost by up to 70 percent for most processes.

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