Downstream Manufacturing Associate

We are supporting a commercial-stage biologics manufacturer in New Jersey that has successfully transitioned into full-scale GMP production following multiple FDA approvals. As part of continued expansion, they are hiring Downstream Manufacturing Associates with prior industry experience to support large-scale biologics manufacturing operations. This role is suited to candidates with 2+ years of hands-on downstream manufacturing experience within a GMP environment. Key Responsibilities Execute downstream manufacturing processes including chromatography, UF/DF, TFF and filtration Operate and maintain process equipment (e.g. ÄKTA systems, filtration skids) Prepare buffers and solutions in accordance with GMP procedures Complete batch records and ensure accurate GMP documentation Support troubleshooting and process execution on the manufacturing floor Collaborate with QA, QC and MSAT teams Requirements Bachelor’s degree in Biology, Biochemistry, Biotechnology or related field 2+ years of downstream manufacturing experience in a GMP environment Strong hands-on experience with chromatography and filtration processes Understanding of GMP documentation and batch execution Ability to work on-site in New Jersey Nice to Have Experience with TFF / UFDF processes Familiarity with ÄKTA chromatography systems Exposure to large-scale biologics or biosimilars manufacturing Experience supporting tech transfer or scale-up activities Why Apply Opportunity to join a commercial biologics manufacturing site with approved products Exposure to large-scale GMP production and advanced downstream processes Clear progression into senior manufacturing or technical roles Growing organisation with continued investment and expansion #J-18808-Ljbffr Global Life Science Hub