Perform pilot-scale downstream purification using column chromatography, UFDF, and filtration.
Set up, operate and maintain downstream laboratory equipment.
Maintain reagent, sample, and consumables inventory.
Follow good documentation practices to maintain accurate records.
Work with Assay Development and Quality Control to coordinate testing.
Work to optimize and revise process protocols to be robust and streamlined.

🎯 Requirements

Bachelor's or advanced degree in chemical/biochemical engineering or related field.
6-8 years of downstream purification experience in pharma or gene therapy GMP ops.
Hands-on with buffer prep, TFF (HF/Cassettes), UF/DF, column chromatography; AKTA Avant.
Team player with strong communication skills in a fast-paced environment.
Proficient in Excel and Word; JMP data analysis is a plus.
Familiarity with regulatory guidelines for biologics manufacturing is a plus.

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Engineering Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot