Proces Development Engineer III, Bioconjugation Development
$109,900–$179,300 year
On-site · Tarrytown, New York, United States
Job Summary
Regeneron's Process Development Engineer III will develop conjugation and purification processes for bioconjugation of proteins, working in collaboration with cross-functional teams to implement Quality by Design (QbD) principles suitable for GMP production. Responsibilities include the scale-up and technology transfer of manufacturing workflows, designing scalable GMP-ready processes, using statistical DOE for optimization, and authoring technology transfer documentation. Candidates should possess strong knowledge of protein purification principles and experience in a laboratory setting, with a preference for bioconjugation and analytical characterization expertise.
Required Qualifications
- Bachelor’s + 10+ years relevant experience or Master’s + 8+ years relevant experience or a PhD + 0-3 years experience in chemical/biochemical engineering or a related field.
- Strong initiative and aim to complete challenging tasks and learn new technologies.
- Strong fundamental understanding of various protein purification and technology transfer principles.
- Excellent interpersonal, verbal and written communication skills.
- Critical thinking and problem-solving skills.
Desired Qualifications
- Experience with antibodies in the bioconjugates space is highly preferable.
- Hands on experience with bioconjugation processes (lysine-based, cysteine-based, site-specific etc.)
- Practical knowledge of downstream purification techniques such as chromatography, ultrafiltration/diafiltration, membrane technologies
- Experience with a variety of analytical characterization tools such as high-performance liquid chromatography (HPLC), UV spectroscopy
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