Avantor - United States, On-site work

Seeking a Regional Lead Administrator for IT Ops and Site Services in Carpinteria. You will manage a technician team, act as the key IT liaison for USA manufacturing sites, and ensure service levels. Requires ITIL expertise, security clearance, and experience with PC, network, and printer technol...

Join Avantor, a Fortune 500 leader, as a Quality Assurance Associate in Paris, KY. This full-time, on-site role requires 2+ years of QA experience in a regulated cGMP/ISO environment. You will ensure compliance, manage documentation, and mentor peers within a dynamic 24/7 operational schedule.

Join Avantor's Biopharma Production team in Bridgewater, NJ as an R&D Associate Scientist. You will conduct experiments and support pilot-scale production in a GLP/GMP environment. This on-site role requires a BS/BA in science and hands-on lab experience. We offer comprehensive benefits, includin...

Join Avantor as a Quality Assurance Specialist in Devens, USA. Ensure quality standards in a dynamic biopharma production environment, reviewing documentation and supporting batch records. Ideal candidates have 1+ years in a regulated industry, GMP knowledge, and strong attention to detail. This ...

Join Avantor as a Quality Inspector in Devens, MA. Ensure biopharma quality standards by inspecting raw materials and documentation in a GMP environment. This full-time role requires 1+ year in a regulated industry and strong attention to detail.

Join Avantor as a Maintenance Technician on the first shift in Carpinteria. You will install, maintain, and repair manufacturing equipment, focusing on gearboxes, pumps, and conveyors. This role requires 1-2 years of industrial experience with electrical, pneumatic, and PLC systems. Ensure operat...