Bioconjugation Process Development & Manufacturing Lead

Role: Bioconjugation Process Development and Manufacturing Lead, responsible for purification process development, technology transfer, scale-up, and GMP manufacturing support of bioconjugate products. Core responsibilities include designing and executing downstream process studies (chromatography, ultrafiltration), leading process transfer from development to GMP, and supporting manufacturing campaigns. Requirements: BS with 5+ years, MS with 3+ years, or PhD with 2+ years of relevant experience; hands-on expertise in chromatography-based purification, process scale-up, and biologics manufacturing in both non-GMP and GMP settings. Preferred skills include GMP compliance knowledge, bioconjugation process experience, and ability to author technical documentation. High-value biopharma specifics: focus on radiopharmaceuticals, late clinical-stage biologics, and supporting clinical and commercial manufacturing. Collaboration involves working with manufacturing, quality control, and process development teams. Work setup is hybrid, with potential radiation safety training; travel not specified.