Nexcella, Inc. Jobs in Canada

+The Cell Therapy Manufacturing Analyst will analyze good manufacturing practice cell therapy manufacturing processes to ensure consistency of product manufacturing, testing, qualification, validation, and performance validation (critical process parameters, critical process attr ...

The Cell Therapy Manufacturing Analyst will analyze good manufacturing practice cell therapy manufacturing processes to ensure consistency of product manufacturing, testing, qualification, validation, and performance validation. · Ensure that timelines are met. · Mitigate risks. ...

A biopharmaceutical company in the Greater Montreal Area is seeking a Clinical Trial Master File (TMF) Manager. The successful candidate will be responsible for managing eTMF completeness checks, ensuring inspection readiness and compliance with FDA regulations, while also leadin ...

The Supplier Quality Management (SQM) role will be responsible for the oversight of external suppliers, · Bachelor's degree in Life Sciences6–8 years of experience in supplier quality management within the pharmaceutical/biotech sector.Strong knowledge of ICH Q10, ICH E6 (R2), an ...

Clinical Trial Master File (TMF) Manager · Greater Montreal Area / Hybrid · Our 3 Core Values · Our mission is to harness the immune system through innovative cell therapies and other modalities to deliver widely accessible cures. Patients are waiting · What You'll Do · As a TMF ...

The Supplier Quality Management (SQM) role will be responsible for the oversight of external suppliers, including Clinical and CMC vendors. · Bachelor's degree in Life Sciences6–8 years of experience in supplier quality management within the pharmaceutical/biotech sector. · ...

The Manager, Quality Engineering & CSV / IT is responsible for oversight of GxP computerized systems validation (CSV) and quality engineering support across clinical and commercial operations. · Oversight of GxP computerized systems validation (CSV) · Quality engineering support ...

Clinical Trial Master File Manager in Greater Toronto Area/Hybrid or Greater Montreal Area/Hybrid responsible for eTMF completeness checks, periodic reviews, cross-checks and identifying missing documents. · Manage eTMFs for allocated studies · Liaise with study teams and other T ...

A biopharmaceutical company in the Greater Montreal Area is seeking a Clinical Trial Master File (TMF) Manager. The successful candidate will be responsible for managing eTMF completeness checks, ensuring inspection readiness and compliance with FDA regulations, while also leadin ...

Nexcella Inc is a subsidiary of Immix Biopharma Inc · ...

Clinical Trial Master File (TMF) Manager · Greater Montreal Area / Hybrid · Our 3 Core Values · Our mission is to harness the immune system through innovative cell therapies and other modalities to deliver widely accessible cures. Patients are waiting · What You'll Do · As a TMF ...

The Manager/Senior Manager, QA Lot Disposition is responsible for independent QA oversight and final disposition for clinical and commercial drug product lots manufactured and tested at external CDMO partners. · ...

We are seeking a Clinical Trial Assistant to join our team at Nexcella Inc., a clinical-stage biopharmaceutical company trailblazing cell therapies in AL Amyloidosis and other serious diseases. · The successful candidate will assist Clinical Research Associates (CRAs) and Regulat ...

The Manager, · Quality Engineering & CSV / IT is responsible for oversight of GxP computerized systems validation · (CSV) and quality engineering support across clinical · and commercial operations, · including external partners as applicable.The role partners closely with QA/QS ...