Labware LIMS Validation Specialist
Listed on 2026-06-27
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Quality Assurance - QA/QC
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Healthcare
Location: Newbury Park
Lab Ware Lims Validation Specialist
Greetings,
I am seeking an experienced Lab Ware Lims Validation Specialist to support a Lab Ware 8 upgrade for a US-based Gmp laboratory site in Ca. This role will focus on validation document generation for a Lab Ware 8 Lims upgrade project and strong liaison with onsite Smes.
9+ month Onsite Contract role in Thousand Oaks, Ca. Contract thru March 2027, with possible extension C2C Pay rate: $80/ hr. hour depending upon experience.
Client name will not be disclosed until after a qualified candidate resume is presented. Two recent work references will be required from candidates upon submission. Resumes will be screened by an Ai tool and blatant Ai generated resumes will be rejected.
Requirements for the Lab Ware Lims Validation Specialist:
- Must have previous experience providing validation document generation for previous Lab Ware Lims upgrades. This must be clearly stated on the resume. Lab Ware 8 Lims upgrade experience highly preferred.
- Strong experience with Labware within Gmp laboratory operations, particularly raw materials testing, commercial product testing and laboratory equipment workflows
- Demonstrated ability to translate regulatory and quality requirements into compliant Lims configurations.
- Experience supporting Lims validation with full requirements-to-configuration-to-validation traceability.
- Experience integrating Lab Ware with instrument systems (e.g., Empower, LabX)
- Experience executing stable & compliant configured workflows in operations.
- Experience working in biopharmaceutical or pharmaceutical Gmp environments preferred.
- Strong cross-functional communication skills in regulated environments.
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