Bioconjugation Process Development & Manufacturing Lead
Listed on 2026-10-11
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Regulatory Compliance Specialist -
Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer, Regulatory Compliance Specialist, Pharma Engineer
Bioconjugation Process Development and Manufacturing Lead, responsible for purification process development, technology transfer, scale‑up, and GMP manufacturing support of bioconjugate products.
Core responsibilitiesDesigning and executing downstream process studies (chromatography, ultrafiltration), leading process transfer from development to GMP, and supporting manufacturing campaigns.
RequirementsBS 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 skillsGMP compliance knowledge, bioconjugation process experience, and ability to author technical documentation.
High‑value biopharma specificsFocus on radiopharmaceuticals, late clinical‑stage biologics, and supporting clinical and commercial manufacturing.
CollaborationInvolves working with manufacturing, quality control, and process development teams.
Work setupHybrid, with potential radiation safety training; travel not specified.
Step into the Bioconjugation Process Development & Manufacturing Lead role at Telix Pharmaceuticals Limited in Angleton, TX, United States and grow with us.
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