Avantor - United States, On-site work

Avantor seeks a Senior Manager of Operations in Paris, KY, to lead plant production, quality, and on-time shipping. This on-site role requires 5+ years of experience in chemical, pharma, or medical device manufacturing, with strong PSM, MOC, and cGMP expertise. You will manage a large team, drive...

Join Avantor, a Fortune 500 leader, as a Quality Assurance Inspector in Solon, OH. This full-time, on-site role requires 3+ years of QA experience in medical device or pharmaceutical industries, with knowledge of cGMP and ISO standards. You will ensure product quality, review documentation, and c...

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...