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Elevatebio

Director, Quality Assurance Operations

2 Days Ago

Waltham, MA, USA

379 Employees

Senior level

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379 Employees

Senior level

Biotech

The Director of QA Operations leads Quality Assurance oversight for cell and gene therapy manufacturing at ElevateBio's BaseCamp facility. This role includes managing a QA team, ensuring compliance with cGMP regulations, implementing quality processes, and collaborating with various departments to enhance product quality and manufacturing efficiency.

Elevatebio

Principal Associate Scientist, Analytical Development (Contractor)

2 Days Ago

Waltham, MA, USA

379 Employees

Mid level

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379 Employees

Mid level

Biotech

The Principal Associate Scientist will support the development and execution of molecular assays and collaborate closely with various teams. Responsibilities include optimizing methods, generating protocol documents, troubleshooting, and participating in the lifecycle management of assays, as well as analyzing and presenting data.

Elevatebio

Manager, Quality Audits

2 Days Ago

Waltham, MA, USA

379 Employees

Expert/Leader

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379 Employees

Expert/Leader

Biotech

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.

Elevatebio

Site Head, BaseCamp Pittsburgh

18 Days Ago

Pittsburgh, PA, USA

379 Employees

Senior level

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379 Employees

Senior level

Biotech

As Site Head for ElevateBio’s BaseCamp Pittsburgh, you will lead operations, develop talent management plans, recruit top talent, manage project teams, ensure compliance, and foster collaboration for successful operational startup by early 2027.

Elevatebio

Senior Manager, CQV

18 Days Ago

Pittsburgh, PA, USA

379 Employees

Senior level

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379 Employees

Senior level

Biotech

The Senior Manager, CQV will oversee the commissioning, qualification, and validation processes for ElevateBio's new cell and gene therapy manufacturing facility. Responsibilities include preparing validation documentation, leading validation activities, managing external contractors, and ensuring compliance with GMP regulations, while coordinating with various engineering and operational teams.