Confirmed on the employer's own hiring board on Nov 3, 2026. First seen by Alion on Nov 3, 2026. QCS Staffing scores A on the Alion truth index.
Support the design, construction, qualification, and startup of upstream and downstream biologics manufacturing equipment.Support technology transfer and commercialisation activities for biologics manufacturing processes.Monitor process performance using CPV, SPC, MVDA, and PAT methodologies to identify trends and drive improvements.Support process investigations, deviations, change controls, process validation, and continuous improvement initiatives.
What you’ll need:
Extensive experience (MSc) or (BSc) experience within biotechnology, pharmaceutical manufacturing, process engineering, MSAT, or technical operations.Strong understanding of biologics manufacturing processes, including upstream cell culture and/or downstream purification.Extensive knowledge of GMP regulations, process validation, quality systems, deviation management, and change control.Experience with process monitoring tools such as CPV, SPC, MVDA, PAT, and statistical analysis software including JMP or Design Expert.
If this assignment is of interest to you, please apply now! #LI-CH3

