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Principal Associate Scientist role at ElevateBio, responsible for developing and executing molecular assays for viral vectors, cell and gene therapy products, and critical components. Cross-functional collaboration and method optimization are key responsibilities of this four-month contract position.

ElevateBio is seeking a QC Specialist I to support QC analytical activities at contract testing laboratories and QC logistics within the company. Responsibilities include reviewing testing protocols, managing shipping logistics, handling internal sample submission processes, and writing stability protocols. The role requires a Bachelor's degree in a technical discipline and 3-5 years of experience in Quality Assurance or Quality Control in biotechnology or pharmaceutical manufacturing.

Join ElevateBio as a Process Engineer II working at BaseCamp, providing technical and process support for manufacturing suites, equipment lifecycle management, and troubleshooting activities. Collaborate with cross-functional teams and ensure adherence to GMP standards and documentation practices.

The Associate Manager, CMC Operations and Program Management at ElevateBio will lead cross-functional activities between various departments, ensuring alignment with corporate goals and timelines. Responsibilities include coordinating program timelines, managing risks, and contributing to the review of KPIs.

The Associate II, QA Operations at ElevateBio is responsible for providing Quality oversight over execution of clinical cell and gene therapy manufacturing for cGMP compliance. Responsibilities include on-the-floor QA oversight, batch record review, compliance risk identification, and more. The role requires a BA/BS degree with minimum of 3 years of experience in pharmaceutical, biotechnology, or biologics operation.

The Associate Scientist will focus on supporting advanced NGS workflows with an emphasis on amplicon sequencing, automation technologies, and working with the Illumina platform to generate high-quality data. Responsibilities include executing NGS workflows, collaborating with bioinformatics, troubleshooting sequencing workflows, and maintaining NGS instruments.

Manage the Quality Systems, Audit, and Compliance program to ensure compliance with internal policies, regulations, and guidelines. Lead internal and external audit processes, coach auditees, monitor CAPAs, and drive continuous improvement. Support client audits, compile quality metrics, and promote a Quality Culture.