Cellares

You'll provide Quality Assurance oversight of validation activities and GMP documentation at a cell therapy manufacturing facility. You'll **interface with cross-functional teams** to maintain high standards in a **regulated environment**.

You'll lead **method transfer and validation** of analytical methods for cell and gene therapies at Cellares, focusing on the Cell Q platform. Your work will directly support **regulatory submissions** like IND, BLA, and MAA filings. This role stands out for its impact on **advanced cell therapy development** in a mission-driven environment.

You'll design and build **Cellares' enterprise data platform** on **Databricks Lakehouse architecture** from the ground up. Your core impact is enabling real-time decision-making, data governance, and AI readiness across engineering, manufacturing, and quality systems. This role is a startup-style builder role with 90% hands-on work and the opportunity to evolve into a foundational data leader.

You'll lead **GMP-critical digital systems** and act as a **bridge between business and IT**, stabilizing and scaling systems for pre-commercial manufacturing readiness. You'll drive root cause resolution and improve audit readiness.

You'll **design and execute experiments** to drive the continuous improvement of Cellares' **cell therapy manufacturing platform**, working cross-functionally with teams like Analytics and Manufacturing. This role offers the chance to **contribute to cutting-edge cell therapy technologies** in a fast-paced environment.

You'll lead **cell therapy process development** efforts to drive continuous improvement of Cellares' advanced manufacturing platform. You'll interface directly with external partners, manage technology transfer, and provide technical leadership. This role stands out for its impact on **platform onboarding** and **cross-functional collaboration** in a mission-driven biotech.

You'll join the **Process Development team** to design and execute experiments for **cell therapy manufacturing platform** development. You'll contribute to technology transfer, method scale-up, and troubleshooting, working in a **fast-paced, mission-driven environment**.

You'll support the design and execution of experiments for **cell therapy manufacturing platform** development. Your work will directly impact **process optimization** and **platform characterization** in a mission-driven team.

You'll lead **Quality Compliance activities** at our Bridgewater site, ensuring adherence to global GMP regulations and **maintaining the Quality Management System**. Your work will directly impact the growth of our cell therapy pipeline.

You'll generate and execute **validation protocols** for proprietary Cell Shuttle and Cell Q equipment, driving harmonization across global sites. You will ensure GMP compliance and mentor junior engineers in a fast-paced, mission-driven environment.

You'll be a key MSAT representative on client projects, **leading technology transfers** into GMP manufacturing facilities. You'll drive **process automation and scalability solutions** to improve reliability, cost-effectiveness, and compliance. This role offers the chance to shape the future of cell therapy manufacturing **in a fast-paced, mission-driven environment**.

You'll support the development and validation of **fully automated QC testing workflows** in a GMP environment. Your core impact will be transferring and optimizing automated test methods for **commercial-scale QC operations**. You'll also provide **runtime operational support** for the Cell Q platform.

You'll join the Process Sciences team to support advanced cell therapy manufacturing. You'll execute processes in R&D and GMP environments, contributing to platform development. This night shift role in a fast-paced, mission-driven **biotech** environment offers hands-on work with **cutting-edge therapies**.

You'll design and implement **automated workflows** for **cell therapy manufacturing QC testing** using liquid handlers and custom hardware. You'll optimize scalability and robustness of end-to-end automated systems while collaborating with cross-functional teams.

You'll perform **preventive maintenance** and **repair of GMP process equipment** at a cell therapy manufacturing facility. Your core impact will be ensuring optimal equipment functionality and compliance. This role offers the chance to work on cutting-edge **cell therapy automation**.

You'll support **cell therapy manufacturing operations** in a GMP environment, handling buffer/media preparation, sample management, and warehouse tasks. Your work directly contributes to **advanced therapies** for patients. This role offers **hands-on training** across manufacturing and warehouse teams.

You'll lead the Quality organization for a **cell therapy manufacturing facility**, ensuring cGMP compliance from launch through commercial production. Your core impact will be developing and executing quality strategies that **enable timely product release to patients**. This role stands out for its **multidisciplinary leadership** across operations, regulatory, and cross-functional teams.

You'll lead the execution of Cellares' enterprise AI strategy, operationalizing AI across GMP systems and business functions. Your core impact will be deploying scalable, compliant AI solutions that drive measurable ROI. This role offers a unique opportunity to shape AI governance in a regulated biotech environment.

You'll lead **electrical design** for advanced cell therapy manufacturing equipment, working with a **cross-functional engineering team**. You'll own control panels, PCBAs, and cabling from concept through validation. This role offers **mentorship** and growth in a fast-paced mission-driven environment.

You'll lead a **cell therapy manufacturing team** in a **cGMP facility**, overseeing production of autologous and allogeneic products. You'll drive cross-functional collaboration to ensure safe, compliant, and timely delivery to patients.

You'll build and lead Cellares' **InfoSec program** as the founding security hire, blending strategic development with hands-on execution. You will **drive compliance with frameworks** like 21 CFR Part 11, SOC 2, and ISO 27001. This role offers a unique opportunity to shape security across **a fast-paced, mission-driven company**.

You'll perform **analytical testing** on cell therapy products in a **cGMP environment** at our Bridgewater, NJ facility. Your work ensures product quality and regulatory compliance for in-process, release, and stability samples. This role offers hands-on experience with advanced assays like dPCR, qPCR, and flow cytometry.

You'll lead enterprise client programs within the Process Development team, managing tech transfer and scaling cell therapy manufacturing onto the **Cell Shuttle platform**. Your work will directly impact **regulatory filings and commercialization** of novel cell therapies. This role offers the chance to shape best practices in a **fast-paced, mission-driven environment**.

You'll design and execute cell therapy process development experiments to advance the Cellares manufacturing platform. You'll interface cross-functionally with Analytical Development, MSAT, Quality, Manufacturing, and Engineering. This role offers the opportunity to drive **continuous improvement** of **autologous and allogeneic cell therapy** processes.

You'll lead **IT/OT operations** in a global cell therapy lab, managing network and security on proprietary equipment. You'll ensure 24x7 uptime and GMP compliance across multiple sites. This role offers the chance to drive system reliability in a fast-paced, mission-driven environment.

You'll support cell therapy manufacturing operations in a GMP environment, working night shifts (11 PM-7:30 AM). You'll execute **routine manufacturing processes**, collaborate with Process Sciences teams, and contribute to **ongoing process improvements**. This role offers hands-on training in a fast-paced biotech setting.

You'll provide **hands-on technical ownership** of automation equipment and control systems for an **advanced cell therapy manufacturing platform**. As the first point of contact for production issues, you'll troubleshoot, sustain, and improve equipment while coaching operators and technicians.