Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. We imagine a world where cancer is a curable disease. 

 At Replimune, we live by our values: 

United: We Collaborate for a Common Goal. 

Audacious: We Are Bold and Innovative. 

Dedicated: We Give Our Full Commitment. 

Candid: We Are Honest With Each Other. 

People are at the center of everything we do, and when it comes to our employees, we make it personal.  With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to contribute to the meaningful work we do which could impact the lives of patients.  

 Join us, as we reshape the future. 

Job Summary: 

Scientist I, Analytical Development is responsible for performing routine analytical testing to support AD, Process Development (PD), Research and Quality Control (QC) projects. Scientist I also provides support to development, optimization, qualification, and validation of analytical methods and AD characterization projects.

This is a fixed-term position for a period of up to one year. Fixed-term employees are eligible Replimune benefits. Position is based in our Milton Park location and typically has a 5-day on-site expectation. 

Key responsibilities:

• Perform in-house in-process and stability testing (PCR, ELISA, chromatography and cell-based analytical tests) to support Process Development, Analytical Development, Research and Quality Control testing.
• Provide support by performing analytical method development and product characterisation projects.
• Prepare laboratory chemical reagents and biological assay standards and controls for use in routine testing and development projects.
• Support the development of robust analytical test methods that are in compliance with regulatory guidelines.
• Execute the qualification and validation of analytical test methods and technology transfer in accordance with ICH and other regulatory guidance’s.
• Involved in the daily operations of the Analytical Development group and actively participates in method troubleshooting and data analysis.
• Oversee and perform internal periodic maintenance, calibration and verification of laboratory equipment.
• Perform general laboratory housekeeping tasks, including maintaining stock levels of laboratory consumables.
• Operate in accordance with Good Manufacturing Practice (GMP), company procedures and health and safety practices.

Other responsibilities

• Drafts and reviews analytical reports and standard operating procedures (SOPs)
• Other duties, as assigned.
• Perform review of assay sheets, lab books and GMP documentation.
• Training team members in equipment usage and maintenance.

Educational requirements:

• Bachelor’s degree in a relevant biological science is required; MSc or PhD preferred.

Experience and skill requirement:

• Minimum 4 years' industry experience, preferably in a cGMP Quality environment
• A self-motivated individual, with good time management and able to work in an organised manner.
• An ability to work independently and as part of a small team, with effective communication and an ability to work flexibly to meet varying workloads.
• Ability to interface effectively with management and other groups or project teams.
• Experience in any of cell culture, ELISA, PCR, chromatography.
• Good IT skills in core applications e.g. Microsoft Word, Excel, Outlook and experience in statistical analysis