Mantell Associates
Process Development Scientist - Downstream
Mantell Associates, Granite Heights, Wisconsin, United States
Process Development Scientist - Downstream
Direct message the job poster from Mantell Associates
Associate at Mantell Associates | Cell & Gene Therapy Mantell Associates is currently partnered with a leading CDMO, who is looking to add a talented and driven Scientist in Downstream Process Development to their team.
In this role you’ll contribute hands‑on to purification, chromatography, filtration, and scale‑up processes, helping advance biologic programs through clinical development and into GMP manufacturing.
Responsibilities
Design, develop, and optimize downstream purification processes (chromatography, filtration / TFF / UF‑DF, polishing steps) for biologics and large molecule drug substances
Perform lab‑scale experiments to define process parameters, yield, impurity removal, buffer exchange, and final product quality
Support scale‑up and tech transfer of downstream processes to pilot and GMP manufacturing; collaborate closely with GMP manufacturing and MSAT teams
Author and review technical reports, SOPs, batch records, and data summaries, ensuring accuracy, completeness, and compliance with regulatory and quality standards
Troubleshoot process challenges and performance deviations; propose corrective actions and process improvements
Work cross‑functionally with Analytical Development, Upstream Process Development, Quality, and Regulatory to ensure downstream processes meet safety, purity, productivity and documentation requirements
Requirements
BSc / MSc / PhD in Biochemistry, Chemical Engineering, Biotechnology, or related field (depending on level) with relevant experience in biologics downstream process development
Hands‑on experience with chromatographic purification systems, filtration (TFF / UF‑DF), buffer formulation and polishing steps
Experience supporting tech transfers or scale‑ups to GMP or pilot‑scale manufacturing environments desirable
Strong experimental design skills, data analysis, problem‑solving, and documentation (SOPs, batch reports, process summaries)
Excellent collaboration, communication, and adaptability skills; ability to work in both lab and production support settings
Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0)20 3854 7700.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Science, Manufacturing, and Quality Assurance
Industries Biotechnology Research, Pharmaceutical Manufacturing, and Chemical Manufacturing
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Associate at Mantell Associates | Cell & Gene Therapy Mantell Associates is currently partnered with a leading CDMO, who is looking to add a talented and driven Scientist in Downstream Process Development to their team.
In this role you’ll contribute hands‑on to purification, chromatography, filtration, and scale‑up processes, helping advance biologic programs through clinical development and into GMP manufacturing.
Responsibilities
Design, develop, and optimize downstream purification processes (chromatography, filtration / TFF / UF‑DF, polishing steps) for biologics and large molecule drug substances
Perform lab‑scale experiments to define process parameters, yield, impurity removal, buffer exchange, and final product quality
Support scale‑up and tech transfer of downstream processes to pilot and GMP manufacturing; collaborate closely with GMP manufacturing and MSAT teams
Author and review technical reports, SOPs, batch records, and data summaries, ensuring accuracy, completeness, and compliance with regulatory and quality standards
Troubleshoot process challenges and performance deviations; propose corrective actions and process improvements
Work cross‑functionally with Analytical Development, Upstream Process Development, Quality, and Regulatory to ensure downstream processes meet safety, purity, productivity and documentation requirements
Requirements
BSc / MSc / PhD in Biochemistry, Chemical Engineering, Biotechnology, or related field (depending on level) with relevant experience in biologics downstream process development
Hands‑on experience with chromatographic purification systems, filtration (TFF / UF‑DF), buffer formulation and polishing steps
Experience supporting tech transfers or scale‑ups to GMP or pilot‑scale manufacturing environments desirable
Strong experimental design skills, data analysis, problem‑solving, and documentation (SOPs, batch reports, process summaries)
Excellent collaboration, communication, and adaptability skills; ability to work in both lab and production support settings
Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0)20 3854 7700.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Science, Manufacturing, and Quality Assurance
Industries Biotechnology Research, Pharmaceutical Manufacturing, and Chemical Manufacturing
#J-18808-Ljbffr