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: The Quality Control (QC) Senior Analyst will be responsible for performing the routine and non-routine QC testing following Standard Operating Procedures (SOPs) and established test methods. They will also perform various laboratory-based activities such as reagent preparation, tissue culture, equipment maintenance, sample receipt and disposal etc. The role also involves getting involved in other tasks such as maintaining sample/reagent/consumable inventory and ordering reagents, writing and updating documents, supporting transfer of new methods and supporting audits and inspections. This position is based in our Milton Park location and typically has a 5-day on-site expectation. Perform QC testing of various routine and non-routine samples according to Standard Operating Procedures (SOPs). Maintain various cell lines on regular basis by revival and passaging at set intervals. Review testing data and records of other operators and data verification for reports. Perform QC sample and material receipt and maintain inventory. Routine equipment maintenance and troubleshooting as required Train other analysts within the department within scope of knowledge where applicable. Write or revise SOPs, protocols, FORMs and update as required. Participate in QC method transfers, qualification, and stability activities. Adhere to current Good Manufacturing Practices (cGMP) and Good Documentation practices (GDP). General lab tasks such as housekeeping, inventory of supplies, order supplies etc. Write deviations related to QC and assist with investigations and other documentation as required. Assist with internal and regulatory agency audits / inspections. Ensure training is kept in GMP compliant state. Education: Degree in Chemistry/Biochemistry/ other related science Required Experience: Minimum 3 years of laboratory-based experience working in similar environment. Competent analytical skills and attention for details. Understanding of GMP requirements Computer literacy (including MS Word and Excel), good communication and organizational skills. Ability to work independently and with others in a team