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Remote Gmp Compliance Jobs (NOW HIRING)

Connexion Systems & Engineering, Inc.

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Sr. Specialist, GMP Quality

Boston, MA · Remote

$60 - $75/hr

Remote * Compensation: $60-$75/hour (weekly hours: 40) * Perm salary expectations: $85K-$100K ... Working knowledge to ensure timely disposition of clinical and commercial products in compliance ...

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Remote Gmp Compliance information

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$31.5K

$98.9K

$207.5K

How much do remote gmp compliance jobs pay per year?

As of Jun 17, 2026, the average yearly pay for remote gmp compliance in the United States is $98,949.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $115,000.00 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.

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.

What is the difference between Remote Gmp Compliance vs Remote Quality Assurance Specialist?

AspectRemote Gmp ComplianceRemote Quality Assurance Specialist
Required CredentialsGMP certifications, life sciences backgroundQuality assurance certifications, life sciences background
Work EnvironmentRegulatory compliance, documentation reviewProduct quality oversight, audits
Employer & Industry UsagePharmaceutical, biotech, medical devicesPharmaceutical, 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.
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What cities are hiring for Remote Gmp Compliance jobs? Cities with the most Remote Gmp Compliance job openings:
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Remote Gmp Compliance jobs near you
Infographic showing various Remote Gmp Compliance job openings in the United States as of June 2026, with employment types broken down into 13% As Needed, 25% Full Time, and 62% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $98,949 per year, or $47.6 per hour.

Sr Quality Manager

Keystone & Golden, Inc.

Lexington, KY • Remote

Full-time

Posted yesterday

Job description

About the Company

Our client is a rapidly growing consumer health and wellness company that has quickly become a category leader in functional oral pouch products. Backed by top-tier consumer investors, industry operators, and professional athletes, the company is redefining performance-focused products through science-backed innovation and premium quality standards.

This is a unique opportunity to join a high-growth organization during a pivotal stage of expansion and help build the quality infrastructure that will support future growth.

Position Summary

The Senior Quality Manager will lead quality systems across the entire supply chain, from raw material suppliers and contract manufacturers to distribution and consumer complaint management.

This is a highly visible "build" role responsible for establishing and scaling quality processes, supplier qualification programs, audit systems, and complaint management procedures that ensure compliance with 21 CFR Part 111 and applicable dietary supplement regulations.

Reporting directly to executive leadership, this individual will serve as the quality subject matter expert and play a critical role in protecting product integrity, regulatory compliance, and consumer trust.

Key Responsibilities

Quality Systems & Compliance

  • Maintain and continuously improve the Quality Management System (QMS), including SOPs, specifications, batch records, deviations, CAPA, and change control processes.
  • Ensure compliance with 21 CFR Part 111 and applicable dietary supplement regulations.
  • Partner with Product Development and Operations on specifications, stability programs, and product release testing.
  • Drive a culture of continuous improvement and quality excellence.

Contract Manufacturer Audits

  • Develop and execute a risk-based audit program across all manufacturing partners.
  • Conduct on-site and remote GMP audits evaluating quality systems, documentation practices, sanitation programs, and manufacturing controls.
  • Issue audit reports, track CAPAs, and verify timely closure of findings.
  • Maintain audit readiness across all operational facilities.

Consumer Complaint Management

  • Build and manage an end-to-end complaint handling system.
  • Establish investigation workflows, escalation procedures, and adverse event reporting processes.
  • Lead root cause investigations and CAPA implementation.
  • Monitor complaint trends and provide actionable insights to Quality, Regulatory, and Product Development teams.

Supplier Qualification

  • Develop and manage supplier qualification and approval programs.
  • Review specifications, Certificates of Analysis, identity testing requirements, and supplier documentation.
  • Conduct supplier risk assessments and maintain Approved Supplier Lists.
  • Manage supplier performance monitoring, requalification activities, and change control processes.

Qualifications

Required

  • Bachelor's degree in Chemistry, Food Science, Microbiology, or related scientific discipline.
  • 5+ years of quality experience within dietary supplements, food, pharmaceuticals, or consumer products.
  • Experience leading or supporting supplier qualification programs and GMP audit initiatives.
  • Strong working knowledge of:
    • 21 CFR Part 111
    • GMP requirements
    • CAPA systems
    • Complaint handling processes
    • Supplier quality management
  • Experience implementing or managing quality tracking and complaint management systems.
  • Strong investigative, problem-solving, and root-cause analysis skills.

Preferred

  • Experience with oral pouch, buccal, or alternative delivery systems.
  • ASQ certifications such as CQA, CQM, CQE, or equivalent.
  • Experience supporting high-growth consumer products or dietary supplement organizations.