LabWare Systems Consultant

The Labware Systems Analyst – QC serves as the primary subject matter expert for the QC Labware LIMS environment. This role supports the full lifecycle of system configuration and enhancement activities, including master data management, system updates, testing, validation, and deployment. The position partners closely with Quality Control, IT, and Digital teams to ensure the LIMS platform effectively supports QC operations, maintains data integrity, and aligns with regulatory expectations.

• →Act as the lead Labware LIMS expert for Quality Control, providing oversight for system configuration, data integrity, change management, and ongoing system maintenance.
• →Maintain in-depth, hands-on expertise in Labware LIMS architecture, including workflows, templates, calculation logic, interfaces, and master data models.
• →Manage end-to-end implementation of Labware system changes, from requirements gathering and functional design through configuration, testing, validation, and production release.
• →Support complex QC initiatives such as new product introductions, method lifecycle activities, and laboratory process improvements.
• →Evaluate and implement new LIMS features, modules, and integrations to streamline laboratory workflows and reduce manual processes.
• →Serve as a key contributor during system design discussions, translating QC business needs into scalable and compliant LIMS solutions.
• →Optimize workflows and user interfaces to ensure accurate data capture, standardized execution of laboratory testing, and seamless integration with enterprise systems.
• →Enable data analytics and digital initiatives by ensuring high-quality, structured data outputs from LIMS and related QC platforms.
• →Collaborate cross-functionally with QC, IT, Digital, Validation, Manufacturing, and Quality Systems teams to deliver compliant and effective LIMS enhancements.
• →Participate in site-level and global quality or informatics forums, representing the QC LIMS function and contributing to best practice sharing.

• Strong hands-on experience configuring and supporting Labware LIMS in a Quality Control laboratory environment.
• Demonstrated experience acting as a system owner or SME for LIMS platforms, including change control, validation support, and lifecycle management.
• Proven ability to design and implement paperless, digital laboratory solutions that automate data capture, calculations, approvals, and system integrations.
• Solid understanding of QC laboratory operations, GxP requirements, and data integrity principles.
• Familiarity with related laboratory informatics systems such as ELN, CDS, MODA, and their integration with LIMS platforms.
• Ability to manage multiple system changes and QC initiatives simultaneously while meeting timelines and compliance expectations.
• Strong problem-solving and analytical skills, with the ability to proactively identify and resolve system, data, or process issues.
• Working knowledge of key QC processes including release testing, stability programs, method validation, and laboratory investigations.
• Capability to translate scientific and operational requirements into robust LIMS configurations and recommend alternative technical solutions when needed.
• Excellent communication and stakeholder management skills, with experience presenting technical topics to cross-functional teams, governance bodies, and audit groups.

Salary Range: $65/Hr. Range varies based on knowledge and experience. Higher rates for short-term assignments and independent contractors. If you are a dedicated Validation Engineer with a passion for ensuring the quality and compliance of manufacturing processes in the biopharmaceutical industry, we want to hear from you! Join us on our mission to revolutionize medicine and transform lives. Apply now to be part of a dynamic team driving innovation in California and beyond.

This is an excellent opportunity to play a key role in advancing digital quality control operations within a regulated, science-driven environment. Apply today!