Bioconjugation Process Development & Manufacturing Lead

Scorpion Therapeutics; Angleton (TX); Hybrid; USD 180,000 - 240,000; Full time

Job summary

Scorpion Therapeutics in Texas is seeking a Bioconjugation Process Development and Manufacturing Lead to drive purification process development, scale-up, and GMP support for bioconjugate products.

You will design and execute downstream studies (chromatography, ultrafiltration), lead technology transfer from development to GMP, and collaborate with manufacturing, quality control, and process development teams in a hybrid work setting.

Qualifications

• BS with 5+ years, MS with 3+ years, or PhD with 2+ years of relevant experience.
• Hands-on chromatography purification, process scale-up, and biologics manufacturing.
• Experience in both non-GMP and GMP settings.

Responsibilities

• Designing and executing downstream process studies (chromatography, ultrafiltration).
• Leading process transfer from development to GMP.
• Supporting manufacturing campaigns and tech transfers.

Skills

Chromatography purification

Process scale-up

Biologics manufacturing

GMP knowledge

Bioconjugation

Technical documentation

Cross-functional collaboration

Education

Bachelor's degree in relevant field

Master's degree in relevant field

PhD in relevant field

Job description

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

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

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

Hybrid, with potential radiation safety training; travel not specified.