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Microbac is seeking a GMP Systems Administrator to take ownership of all GMP software validations and lab IT system compliance activities across our regulated laboratory environments. This role is essential in ensuring that all computerized systems—including laboratory instrumentation software—are validated, maintained in a state of control, and fully compliant with applicable regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5). The ideal candidate will have deep experience in GMP software validation, supporting laboratory instrument systems, and preferably hands-on familiarity with chromatography data systems (CDS) such as Chromeleon, or equivalent. This role bridges IT systems administration with quality and regulatory oversight, working closely with laboratory staff, QA, and vendors to implement and maintain compliant, validated systems fit for use in a GMP environment. This is a six-month position, with potential for full-time employment.
