Remote (California-Based Project) Duration: Through March 2027 (Potential Extension) Position ... Design, configure, and optimize laboratory workflows while ensuring compliance with GMP and ...
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Remote (California-Based Project) Duration: Through March 2027 (Potential Extension) Position ... Design, configure, and optimize laboratory workflows while ensuring compliance with GMP and ...
Document Control Specialist
Irvine, CA · On-site +1
$23 - $25/hr
Reviews document format to ensure compliance to Good Documentation Practices (GDPs). * Assists in ... Remote or hybrid arrangements are not available. Employment Type: full-time
Document Control Specialist
Irvine, CA · On-site +1
$23 - $25/hr
Reviews document format to ensure compliance to Good Documentation Practices (GDPs). * Assists in ... Remote or hybrid arrangements are not available. Employment Type: full-time
Remote Gmp Compliance information
See Riverside, CA salary details
$32.9K - $49.6K
10% of jobs
$63K is the 25th percentile. Wages below this are outliers.
$49.6K - $66.2K
19% of jobs
$66.2K - $82.9K
19% of jobs
The median wage is $85K / yr.
$82.9K - $99.6K
17% of jobs
$111K is the 75th percentile. Wages above this are outliers.
$99.6K - $116.3K
15% of jobs
$116.3K - $133K
6% of jobs
$133K - $149.7K
5% of jobs
$149.7K - $166.4K
3% of jobs
$166.4K - $183.1K
2% of jobs
$183.1K - $199.8K
2% of jobs
$199.8K - $216.5K
1% of jobs
$32.9K
$103.2K
$216.5K
How much do remote gmp compliance jobs pay per year?
As of Jul 28, 2026, the average yearly pay for remote gmp compliance in Riverside, CA is $103,231.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,200.00 and $120,000.00 per year, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a Remote GMP Compliance professional, and why are they important?
To thrive as a Remote GMP Compliance professional, you need a solid understanding of Good Manufacturing Practices, quality assurance principles, and relevant regulatory requirements, typically backed by a degree in life sciences or a related field. Familiarity with compliance management software, electronic document management systems, and industry certifications such as Six Sigma or ASQ are highly valuable. Strong attention to detail, excellent communication, and problem-solving abilities help you effectively ensure compliance and facilitate remote audits. These skills and qualifications are crucial for maintaining product quality, regulatory adherence, and organizational integrity in remote and distributed work environments.
Can regulatory affairs jobs be done remotely?
Regulatory affairs jobs, including roles focused on GMP compliance, can often be performed remotely, especially with the use of digital documentation, communication tools, and compliance management software. However, some tasks may require onsite presence for inspections, audits, or laboratory work, depending on company policies and regulatory requirements.
What is the career path for compliance?
A career in remote GMP compliance typically starts with an entry-level role such as compliance associate or specialist, focusing on understanding regulations and documentation. Progression can lead to senior compliance roles, managerial positions, or specialized areas like quality assurance or regulatory affairs, often requiring relevant certifications and experience with regulatory agencies like the FDA.
What is a Remote GMP Compliance specialist?
A Remote GMP Compliance specialist is a professional responsible for ensuring that a company’s manufacturing processes, particularly in pharmaceuticals, biotechnology, or food production, follow Good Manufacturing Practice (GMP) regulations while working remotely. They review documentation, conduct virtual audits, help implement compliance protocols, and provide guidance to ensure products meet safety and quality standards. This role requires knowledge of relevant regulations, attention to detail, and strong communication skills to work effectively with onsite teams from a remote location.
How to become a remote compliance analyst?
To become a remote GMP compliance analyst, candidates typically need a bachelor's degree in life sciences, pharmacy, or a related field, along with experience in regulatory compliance or quality assurance. Certifications such as RAC or CQE can enhance prospects, and strong knowledge of GMP regulations, audit skills, and proficiency with compliance management tools are important. Prior experience in pharmaceutical or biotech industries and the ability to work independently are also valuable for remote roles.
What is the difference between Remote Gmp Compliance vs Remote Quality Assurance Specialist?
| Aspect | Remote Gmp Compliance | Remote Quality Assurance Specialist |
|---|---|---|
| Required Credentials | GMP certifications, life sciences background | Quality assurance certifications, life sciences background |
| Work Environment | Regulatory compliance, documentation review | Product quality oversight, audits |
| Employer & Industry Usage | Pharmaceutical, biotech, medical devices | Pharmaceutical, biotech, medical devices |
Remote Gmp Compliance focuses on ensuring adherence to Good Manufacturing Practice regulations, primarily handling compliance documentation and regulatory submissions. Remote Quality Assurance Specialists oversee product quality, conduct audits, and implement quality systems. While both roles require similar industry knowledge and certifications, Gmp Compliance emphasizes regulatory adherence, whereas QA Specialists focus on product quality assurance processes.
What are some common challenges faced by Remote GMP Compliance professionals and how can they be addressed?
Remote GMP Compliance professionals often face challenges such as maintaining clear communication with on-site teams, ensuring up-to-date documentation, and staying current with regulatory changes. To address these issues, it's important to establish regular virtual check-ins, use secure document management systems, and participate in ongoing training. Additionally, building strong relationships with cross-functional teams and leveraging compliance software can help ensure processes remain efficient and compliant, even when working remotely.
What are popular job titles related to Remote Gmp Compliance jobs in Riverside, CA? For Remote Gmp Compliance jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Remote Gmp Compliance jobs in Riverside, CA look for? The top searched job categories for Remote Gmp Compliance jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Remote Gmp Compliance jobs? Cities near Riverside, CA with the most Remote Gmp Compliance job openings:
Contractor
Posted 23 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.