Replimune is pioneering oncolytic immunotherapies to activate robust, long-lasting anti-tumor responses, aiming to revolutionize cancer treatment and envision a future where cancer is curable.
Woburn, MA
Replimune's mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response. Replimune is pioneering the development of novel oncolytic immunotherapies. We imagine a world where cancer is a curable disease.
On-site · Montréal
Design, construct, characterize, and test novel HSV-derived oncolytic virus candidates, while managing virus materials, methods, and non-GMP production. Support cross-functional research and regulatory activities through technical input, data analysis, documentation, and, if required, team management and mentorship.
On-site · Montréal
Administer and maintain laboratory computerized systems in a regulated GxP environment, including access, configuration, lifecycle records, upgrades, troubleshooting, security, and data integrity. Coordinate quality and validation activities, vendor and project work, audits, training, and continuous improvement to keep systems compliant and in a validated state.
On-site · Montréal
Lead the Process Development group at the Milton Park facility, overseeing safe, efficient, compliant laboratory work and production of materials for quality control, assay, preclinical, and toxicology needs. Drive cGMP process improvements and ensure development, characterization, and technology-transfer work is documented, reported, and archived appropriately.
On-site · Montréal
Perform routine and non-routine quality control testing, maintain cell lines and laboratory equipment, and manage samples, materials, and inventory. Support method transfers, validations, stability activities, documentation, investigations, training, and internal or regulatory audits while following GMP and GDP requirements.
On-site · Montréal
The Scientist I is responsible for performing routine analytical testing including PCR, ELISA, and chromatography to support process and analytical development. They also contribute to method validation, troubleshooting, and the maintenance of laboratory equipment in compliance with GMP standards.
On-site · Montréal
The Analyst II performs routine analytical testing including PCR, ELISA, and chromatography to support development and quality control projects. They are also responsible for laboratory maintenance, equipment calibration, and ensuring compliance with GMP standards.
Hybrid · Montréal
The Qualified Person is responsible for certifying and releasing batches of clinical and commercial products in compliance with EU and UK GMP laws. This includes overseeing batch reviews, managing quality defects, and ensuring the entire supply chain meets regulatory specifications.
On-site · Montréal
The Scientist I will perform QC testing according to cGMP standards and manage laboratory systems, equipment, and junior staff. They will also lead assay transfers, validation activities, and participate in regulatory inspections and lab investigations.
On-site · Montréal
The Scientist I will perform QC testing according to cGMP standards and manage laboratory systems, equipment, and junior staff. They will also lead assay transfers, validation activities, and participate in regulatory inspections and lab investigations.
On-site · Montréal
The Quality Control Technician will support daily laboratory operations by performing reagent preparation, equipment maintenance, and sample management. They will also assist with data verification and general laboratory housekeeping tasks.
