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The QC Technical Writer II will support Lab Compliance and Continuous Improvements by completing quality event records, conducting root cause investigations, and assisting with CAPA and Change Control processes. This role requires collaboration with various QC and analytical teams and involves training laboratory staff.

The Director of MSAT at ElevateBio will lead process performance qualification and commercial readiness activities for genomic therapies. Responsibilities include overseeing compliance with regulatory standards, establishing process validation frameworks, collaborating with cross-functional teams, and managing a team of engineers. The role focuses on delivering commercial batches and supporting regulatory submissions.

The Associate II in Analytical Testing Core will perform non-GMP assays to support research and manufacturing efforts. Responsibilities include managing sample receipt, executing tests, drafting SOPs, maintaining inventory, and ensuring timely data reporting.

As a Process Engineer Contractor at ElevateBio, you will provide technical support for GMP manufacturing, technology transfers, and validation projects. Key responsibilities include authoring technical documentation, conducting root cause analysis, supporting process validation, and collaborating across functions to enhance manufacturing processes.

The Senior MES Engineer will manage and optimize Manufacturing Execution Systems, leading a team of engineers, handling multiple tech transfer projects, and ensuring smooth transitions between MES systems. Responsibilities include project planning, developing standards for documentation, and supporting system upgrades. The role demands strong project management skills and GxP manufacturing experience.

The Process Engineer II will provide technical support and troubleshooting for manufacturing processes in a GMP biotech facility. Responsibilities include managing equipment lifecycle, resolving technical issues, and collaborating with cross-functional teams for process optimization and compliance with regulatory standards.

As a QC Specialist I at ElevateBio, you will support QC analytical activities and logistics, review assay protocols, analyze data from contract labs, manage sample submissions, and handle stability data and reports.