Biopharma Downstream Operator - cGMP/Validation; Day Shift
Listed on 2026-10-08
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Production Associate / Production Line -
Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer
Scorpion Therapeutics is hiring a Manufacturing Associate for biopharma drug substance production, focusing on downstream purification like chromatography, viral filtration, and ultrafiltration. You will operate process equipment and follow strict cGMP guidelines.
Day shift (6 AM–6 PM ET) on a 2-2-3 rotation, with emphasis on training, safety, and seamless production in a fast-paced, 24/7 RTP facility.
We are currently recruiting a Biopharma Downstream Operator - cGMP/Validation (Day Shift) for our team in NC, United States.
This is a strong role to take on the Biopharma Downstream Operator - cGMP/Validation (Day Shift) role at Scorpion Therapeutics.
As a Biopharma Downstream Operator - cGMP/Validation (Day Shift), you will play an important part at Scorpion Therapeutics in NC, United States.
We invite applications for the Biopharma Downstream Operator - cGMP/Validation (Day Shift) position located in NC, United States.
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