ZipRecruiter

Log In

2

Remote Validation Jobs in Riverside, CA (NOW HIRING)

next page

Showing results 1-20

All JobsValidation JobsRemote Validation JobsRemote Validation Jobs in Riverside, CA

Remote Validation information

See Riverside, CA salary details

$23

$54

$81

How much do remote validation jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for remote validation in Riverside, CA is $54.25, according to ZipRecruiter salary data. Most workers in this role earn between $41.11 and $65.96 per hour, depending on experience, location, and employer.

What are common challenges faced in a Remote Validation role and how are they addressed?

One of the most common challenges in a Remote Validation position is ensuring thorough communication and documentation when coordinating with on-site teams and cross-functional colleagues. To overcome this, professionals in this role rely heavily on detailed reporting, frequent virtual meetings, and collaborative project management tools to maintain alignment and transparency. Adapting validation strategies to a remote environment also requires a strong understanding of digital validation tools and best practices for remote audits. Regular training and clear standard operating procedures can help keep validation processes efficient and compliant, even when working off-site.

What are the key skills and qualifications needed to thrive in the Remote Validation position, and why are they important?

To thrive in Remote Validation, you need a solid background in quality assurance, process validation, and regulatory compliance, often supported by a degree in engineering, life sciences, or a related field. Familiarity with validation protocols, statistical analysis software, and documentation systems like TrackWise is highly valuable, along with certifications such as Six Sigma or ASQ. Excellent attention to detail, strong communication skills, and the ability to work independently are critical soft skills. These competencies ensure rigorous validation processes, effective remote collaboration, and compliance with industry standards.

What is a Remote Validation job?

A Remote Validation job involves ensuring that systems, software, or processes meet specified requirements and function correctly, typically in regulated industries like pharmaceuticals, healthcare, or manufacturing. Professionals in this role conduct tests, analyze data, and document compliance, all while working remotely. They may validate software applications, equipment, or processes to meet regulatory standards such as FDA, ISO, or GMP guidelines. Strong attention to detail, knowledge of validation protocols, and proficiency with industry regulations are essential for success in this role.

What are popular job titles related to Remote Validation jobs in Riverside, CA? For Remote Validation jobs in Riverside, CA, the most frequently searched job titles are:
What cities near Riverside, CA are hiring for Remote Validation jobs? Cities near Riverside, CA with the most Remote Validation job openings:
Remote Validation jobs near you

LabWare 8 LIMS Configuration & Integration Specialist

Stark Pharma Solutions Inc

Irvine, CA • Remote

Contractor

Posted 10 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Role: LabWare 8 LIMS Configuration & Integration Specialist

Location: Remote (California-Based Project)

Duration: Through March 2027 (Potential Extension)

Position Overview

We are seeking an experienced LabWare 8 LIMS Configuration & Integration Specialist to support a large-scale LabWare 8 upgrade initiative within a GMP-regulated pharmaceutical laboratory environment. This role will lead critical workstreams focused on configuring raw material and commercial product testing workflows, master data management, equipment integration, and validation support.

The ideal candidate will have extensive hands-on experience with LabWare 8 configuration, laboratory system integrations, and GMP laboratory operations, with the ability to deliver compliant and scalable LIMS solutions.

Key Responsibilities

  • Configure and implement LabWare 8 LIMS workflows supporting raw material and commercial product testing processes.
  • Lead master data configuration and management activities to support laboratory operations.
  • Design, configure, and optimize laboratory workflows while ensuring compliance with GMP and regulatory requirements.
  • Support integration of LabWare 8 with laboratory instrumentation and enterprise systems.
  • Collaborate with Quality, Validation, Laboratory Operations, and IT teams to ensure successful project execution.
  • Translate business, quality, and regulatory requirements into compliant LIMS configurations.
  • Support system validation activities, ensuring complete requirements-to-configuration-to-validation traceability.
  • Troubleshoot configuration, workflow, and integration issues while driving timely resolution.
  • Assist with user acceptance testing (UAT), system testing, and deployment activities.
  • Support inspection readiness efforts and ensure compliance with regulatory expectations for computerized systems.
  • Provide technical guidance and documentation throughout the project lifecycle.

Required Qualifications

  • 8+ years of experience working with Laboratory Information Management Systems (LIMS).
  • Strong hands-on experience configuring and implementing LabWare 8 LIMS.
  • Proven experience supporting LabWare upgrades, implementations, or enhancement projects.

Experience configuring workflows for:

  • Raw Material Testing
  • Commercial Product Testing
  • Laboratory Equipment and Instrument Workflows
  • Demonstrated experience supporting GMP-regulated laboratory environments.
  • Experience integrating LabWare with laboratory instruments and enterprise systems.
  • Strong understanding of computerized system validation (CSV) principles and documentation requirements.
  • Experience supporting validation deliverables with end-to-end traceability.
  • Excellent communication and stakeholder management skills within regulated environments.