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???????????????? ???????????????????????????????????????????? & ???????????????????????????????????????? ???????????????????????????????? (???????????????????????????? ????????????????)

Job

MSR Technology Group

Thousand Oaks, CA (In Person)

Full-Time

Posted 5 days ago (Updated 1 day ago) • Actively hiring

Expires 7/22/2026

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Job Description

???????????????? ???????????????????????????????????????????? & ???????????????????????????????????????? ???????????????????????????????? (???????????????????????????? ????????????????) at MSR Technology Group ???????????????? ???????????????????????????????????????????? & ???????????????????????????????????????? ???????????????????????????????? (???????????????????????????? ????????????????) at MSR Technology Group in Thousand Oaks, California Posted in about 24 hours ago.
Type:
full-time
Job Description:
Title:
???????????????? ???????????????????????????????????????????? & ???????????????????????????????????????? ???????????????????????????????? (???????????????????????????? ????????????????) ????????????????????????????????: ???????????????????????????????? ????????????????, ???????? (????????????????????????) ????????????????????????????????: 12 ???????????????????????? ???????????????????????????????? We are seeking a LIMS Integration & Validation Engineer with strong hands-on experience in LabWare LIMS to support laboratory digital transformation initiatives in a regulated pharmaceutical environment. This role is ideal for someone who can immediately contribute to LIMS implementation, validation, and instrument integration in a QC laboratory setting. ???????????? ???????????????????????????????????????????????????????????????? Support LIMS migration and laboratory digital transformation initiatives Perform end-to-end GxP validation (URS, IQ, OQ, PQ, Traceability Matrix) Lead instrument-to-LIMS integration for laboratory systems Work closely with QC, IT, and Laboratory teams Ensure compliance with GMP and Data Integrity (ALCOA+) Support change controls, testing, and system lifecycle activities Drive automation of laboratory workflows and processes ???????????????????????????????? ???????????????????????? 5+ years experience in pharmaceutical / biotech / regulated lab environment Strong hands-on experience with LabWare LIMS Experience in GxP Validation (IQ/OQ/PQ, URS, UAT) Laboratory instrument integration experience Strong knowledge of GMP, Data Integrity, ALCOA+ Experience working with QC / analytical laboratory systems