Lims Manager Jobs in Missouri (NOW HIRING)

Job Title: LIMS Data Migration Specialist

Job Description

This role leads and executes Laboratory Information Management System (LIMS) data migration and configuration activities within a GMP-regulated laboratory environment. The specialist ensures accurate migration, validation, and configuration of laboratory master data, supports system implementation from early design through deployment, and partners closely with quality and project teams to achieve critical milestones for a high-profile, multi-year project.

Responsibilities

• Lead and execute LIMS data migration activities, including planning, extraction, transformation, loading, and verification of laboratory data.
• Configure and validate LIMS tables, tests, specifications, and workflows to support laboratory operations and quality requirements.
• Review and verify migrated laboratory data for accuracy, completeness, and alignment with laboratory workflows and documentation standards.
• Support User Acceptance Testing (UAT) activities by preparing test scenarios, executing tests, documenting results, and resolving issues.
• Contribute to system verification efforts to ensure the LIMS environment meets regulatory, quality, and operational requirements.
• Assist with the development and maintenance of Standard Operating Procedures (SOPs), work instructions, and implementation documentation related to LIMS and data migration.
• Partner with Quality Control (QC), Quality Assurance (QA), and project leadership to ensure project milestones are met and deliverables are completed on schedule.
• Participate in troubleshooting and resolution of data migration, configuration, and validation issues within the LIMS environment.
• Support implementation readiness activities leading up to launch, including data readiness checks, user preparation, and system validation tasks.
• Collaborate with laboratory analysts and project team members to understand laboratory workflows and ensure the LIMS configuration supports operational needs.
• Maintain strong documentation and data integrity practices in accordance with GMP requirements and internal quality standards.

Essential Skills

• Bachelor’s degree in a scientific discipline preferred.
• 3–5+ years of experience in pharmaceutical, biologics, veterinary pharmaceutical, or GMP-regulated laboratory environments.
• Previous LIMS implementation experience, including configuration, validation, or deployment activities (beyond end-user experience).
• Hands-on experience performing data migration, configuration, validation, or implementation activities for laboratory systems.
• Strong Excel skills, including use of formulas, data management, and data manipulation for large or complex datasets.
• Understanding of laboratory workflows, specifications, testing, and documentation practices.
• Working knowledge of GMP requirements and data integrity principles in a pharmaceutical manufacturing or regulated laboratory environment.
• Experience supporting master data setup and system configuration in laboratory or quality systems.
• Experience with laboratory system validation activities, including documentation and execution of validation protocols.
• Ability to collaborate effectively with QC, QA, and cross-functional project teams to meet project objectives.

Additional Skills & Qualifications

• Experience supporting system implementation from early-stage design through deployment.
• Familiarity with User Acceptance Testing (UAT) processes and system verification activities.
• Ability to contribute to SOP development, work instructions, and implementation documentation.
• Strong attention to detail and accuracy when working with complex laboratory data.
• Comfort working in a high-profile, multi-year project environment with evolving systems and procedures.
• Excellent communication skills to interact with laboratory analysts, project team members, and quality functions.
• Demonstrated ability to troubleshoot and resolve issues related to data migration and system configuration.

Job Type & Location

This is a Contract position based out of Bridgeton, MO.

The pay range for this position is $35.00 - $60.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a hybrid position in Bridgeton,MO.

This position is anticipated to close on Aug 10, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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