Manufacturing Associate I

Role: Manufacturing Associate I/II supporting cGMP biopharma manufacturing of Replimune’s oncolytic immunotherapies at the Framingham, MA facility. Objectives: execute manufacturing operations, ensure GMP compliance, support process validation, and maintain production readiness. Responsibilities: author SOPs and batch records, perform aseptic gowning, operate viral production equipment (e.g., tangential flow filtration, chromatography), prepare buffers, perform visual inspection, and assist with equipment setup, maintenance, and validation. Qualifications: Bachelor's degree with 1-3 years or Associate’s/High School Diploma with 3-6 years of cGMP biopharma manufacturing experience; experience in cell culture, purification, or aseptic filling; familiarity with single-use technologies; strong organizational, communication, and teamwork skills; proficient in Microsoft Word and Excel. HighValue: biologics manufacturing, viral vector or oncolytic platforms, GMP environment, equipment validation, aseptic processing, and working in a cleanroom setting. Work setup: primarily on-site with some weekend/holiday work depending on production needs.