Cellectis Jobs in United States

Job Description · The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities to ensure compliance with FDA, EMA, ICH, and other applicable ...

The Process Engineer III will be responsible to provide specialist knowledge and expertise of specific cell and gene therapy processes and/or process technologies.This position will also oversee processes and standards to maintain and improve existing and to implement new innovat ...

A leading biotechnology company in New York is seeking a Senior Director, Medical Monitor in Hematology–Oncology. This pivotal role involves guiding clinical strategy, ensuring patient safety, and providing medical oversight for clinical studies. The ideal candidate will hold an ...

The Director Clinical Quality Assurance establishes and leads Clinical QA function providing independent oversight of Good Clinical Practices activities ensuring compliance across Cellectis clinical programs. · ...

Director of Business IT Services · This strategic role will lead global enterprise systems landscape with a focus on Oracle Fusion ERP, PMO, SOX compliance and GMP-regulated environments. · Lead Oracle Fusion ERP strategy implementation and optimization across finance supply chai ...

We are seeking a Senior Director, Medical Monitor with deep Hematology/Oncology expertise to join our Clinical Sciences team and help shape the next generation of UCART therapies.Cellectis is a clinical-stage biotechnology company developing off-the-shelf UCART allogeneic CAR-T t ...

The Sr. Manager/Assoc. · Director, Validation, · Bachelors or Masters in biological or chemical sciences, · Cellectis Raleigh's overall validation program for equipment, · facilities and utilities, control and/or data recording systems, · ...

Position Responsibilities: Assist in responding to site during normal business hours and potentially off-hours and weekends to maintain operations as needed. Manage equipment reliability throughout the entire life cycle of the asset from design and installation through commission ...

This role is responsible for the execution, accountability, and ownership of Metrology activities at the Cellectis, Raleigh, NC facility. Responsible for maintaining an audit ready metrology program in support of clinical and commercial manufacturing. · This role requires a deep ...

Manage equipment reliability throughout the entire life cycle of the asset from design and installation through commissioning and operations to the end of its useful life. · ...

Cellectis' Clinical Sciences team is seeking a highly motivated and experienced Clinical Sciences and Medical Monitor to support the clinical development and execution of our innovative, proprietary UCART allogeneic CAR-T cell therapies. · Reporting to the Chief Medical Officer ...

Job Summary: · The Manufacturing Operations Associate III will be responsible for processes such as cell/tissue culture and manipulation using aseptic techniques. · Cryopreservation of cellular products using DMSO solution and controlled-rate freezers · Perform any and all requir ...

Job summary · The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities to ensure compliance with FDA, EMA, · ICH,and other applicable glo ...

Job Title · Senior Director, Medical Monitor, Hematology–Oncology · Location: New York, NY (Hybrid) · Department: Clinical Development – Clinical Sciences · Reports to: Chief Medical Officer · Overview · Cellectis is a clinical‑stage biotechnology company developing off‑the‑shelf ...

Cellectis' Clinical Sciences organization is seeking a highly motivated and experienced clinical Research Scientist to support the development and execution of our innovative proprietary UCART allogeneic CART cell therapies programs. · The Director, Clinical Research Scientist pa ...

This position is responsible for managing the facilities of a pharmaceutical manufacturing environment. The Senior Manager will oversee equipment reliability and maintenance operations. · Assist in responding to site during normal business hours and potentially off-hours and week ...

Responsibilities · Assist in responding to site during normal business hours and potentially off-hours and weekends to maintain operations as needed. · Manage equipment reliability throughout the entire life cycle of the asset from design and installation through commissioning an ...

Job Description · The Director Clinical Quality Assurance is responsible for establishing and leading the Clinical QA function providing independent oversight of Good Clinical Practices activities ensuring compliance with FDA EMA ICH and other applicable global national regulator ...

We are seeking a Senior Director, Medical Monitor with deep Hematology/Oncology expertise to join our Clinical Sciences team and help shape the next generation of UCART therapies. · MD or DO required · Board certification/eligibility in Hematology and/or Oncology strongly preferr ...

Metrology/Facilities Technician · Responsible for maintaining an audit-ready metrology program supporting clinical and commercial manufacturing. · Execute GMP instrumentation maintenance and calibration activities. · Perform duties including calibration, troubleshooting, maintena ...