Senior, IT GXP Systems Specialist

Role: Senior IT GxP Systems Specialist supporting GxP laboratory, manufacturing, and regulatory systems in a biopharma environment. Responsibilities: manage day-to-day operations, system deployment, upgrades, and validation of GxP compliant systems in line with 21 CFR part 11, including laboratory equipment and networked/stand-alone devices; create documentation, SOPs, and perform troubleshooting; coordinate with vendors and support 24/7 operations. Requirements: Bachelor's in IT, Computer Science, Engineering or equivalent with 4+ years of systems administration experience supporting end-users, servers, and GxP systems; knowledge of Windows, networking protocols, and FDA cGMP/cGLP regulations; strong troubleshooting, incident management, and communication skills. Preferred: 1+ years supporting GxP IT in a pharmaceutical setting. HighValue: GxP validated systems, 21 CFR part 11 compliance, laboratory/manufacturing IT support, on-site role with flexible hours, includes after-hours support and on-call duties.