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Remote Pharmaceutical Quality Assurance Jobs (NOW HIRING)

Dane Street, LLC

Pharmacy QA Specialist

This role is responsible for coordinating with clients, pharmacists, and internal teams to ensure ... Apple equipment and a media stipend are provided for remote workspace. ABOUT DANE STREET: A fast ...

Mitsui Chemical America

QA Manager

New York, NY · Remote

$88K - $130K/yr

Location: Remote, US Department: QA/RC - Corporate Planning Division Reports To: QA/RC Director Are you ready to elevate product quality and reliability? We are seeking an experienced ...

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site +1

Open to Hybrid in Chicago or Remote candidates Key Responsibilities & Core Ownership Champion ... pharmaceutical CRO clinical operations, and proprietary medical device sponsored studies. Empower ...

Travere

Director, Quality Assurance - Technical

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Strong professional experience in a similar role within the pharmaceutical industry, preferably ...

ELB Learning

Quality Assurance Specialist

$45K - $55K/yr

Remote (United States) Job Type: Full-Time Salary: $45,000-$55,000 annually About ELB Learning At ... We're looking for a detail-oriented Quality Assurance Specialist who is passionate about ensuring ...

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How much do remote pharmaceutical quality assurance jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for remote pharmaceutical quality assurance in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

What is a remote pharmaceutical quality assurance?

A Remote Pharmaceutical Quality Assurance job involves ensuring that pharmaceutical products meet regulatory, safety, and quality standards while working from a remote location. Responsibilities may include reviewing documentation, conducting audits, and ensuring compliance with Good Manufacturing Practices (GMP). Professionals in this role collaborate with cross-functional teams to identify quality issues and implement corrective actions. Strong attention to detail, knowledge of regulatory guidelines, and communication skills are essential. Remote QA roles are becoming more common as companies embrace digital workflows and virtual collaboration tools.

What are the main challenges of working remotely in pharmaceutical quality assurance?

Remote Pharmaceutical Quality Assurance professionals often face challenges related to effective communication, real-time document management, and staying up-to-date with facility processes while working off-site. To overcome these hurdles, you’ll need to be comfortable with digital collaboration tools and proactive in reaching out to on-site colleagues when clarifications are needed. Time management and self-discipline are essential to keep up with multiple documentation reviews, virtual audits, and regulatory deadlines. However, many employers provide comprehensive remote training, robust communication platforms, and clear remote workflow protocols to support your success in this role.

What are the key skills and qualifications needed to thrive in remote pharmaceutical quality assurance?

To thrive as a Remote Pharmaceutical Quality Assurance professional, you'll need a deep knowledge of GMP regulations, pharmacological principles, and quality control processes, generally supported by a degree in pharmacy, chemistry, or a related field. Familiarity with quality management systems (QMS), auditing software, and certifications like ASQ CQE or ISO 9001 are highly valuable. Strong attention to detail, effective communication, and self-motivation are key soft skills in this remote setting. These skills ensure regulatory compliance, product quality, and seamless coordination across distributed teams.

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Remote Pharmaceutical Quality Assurance jobs near you
Infographic showing various Remote Pharmaceutical Quality Assurance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

Sr. Quality Assurance Specialist

Sterling Engineering Inc.

North Chicago, IL • On-site, Remote

$40/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Posted yesterday

New

Job description

Job Title: Senior Quality Assurance Specialist | Pharmaceuticals
Location: North Chicago, IL
Hire Type: Long-term contract position (1 year +)
Pay Rate: $40.00/hour
Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), & ESOP
Work Schedule: Hybrid | Remote Monday & Friday; On-Site Tuesday–Thursday | 8:00 AM–5:00 PM
Travel: Up to 20%

Job Summary:
We are seeking a Senior Quality Assurance Specialist to provide Quality Assurance support for a pharmaceutical manufacturing project. This role will support a new project for a key product and ensure product, process, and system-related quality activities comply with applicable corporate and governmental regulations.
The Senior QA Specialist will lead and coordinate Quality projects across multiple site QA functions, manage project deliverables and metrics, identify and mitigate risks, and provide project updates to site management.

Must-Have Skills:
  • Quality Systems: Strong understanding of pharmaceutical Quality Systems and compliance requirements.
  • Communication: Excellent verbal and written communication skills with the ability to work across multiple QA functions.
  • Project Management: Experience planning, coordinating, and driving Quality projects from initiation through completion.
  • Aseptic Processing: Familiarity with aseptic manufacturing processes and associated quality requirements.
  • Combination Products: Experience or familiarity with combination product environments.
Job Duties:
  • Develop, coordinate, and drive execution of Quality projects across multiple site QA areas.
  • Coordinate with site QA planners to achieve project deliverables and timelines.
  • Support deployment of global pharmaceutical Quality initiatives across the site.
  • Analyze and maintain data related to cycle times, touch times, tasks, and processes to improve QA performance.
  • Support development and maintenance of QA planning and scheduling activities.
  • Implement and maintain visual management tools to monitor key QA processes and performance.
  • Analyze and report metrics for planned and unplanned QA activities.
  • Identify project and process risks and develop mitigation or contingency strategies.
  • Lead development of Project Charters, project objectives, requirements, and success criteria.
  • Support regulatory inspections related to new market introductions.
  • Lead or coordinate Compliance and Performance Improvement projects and provide project status updates to site management.
  • Maintain effective relationships with internal Quality functions and third-party contractors.
Qualifications:
  • Bachelor's degree in Science, Engineering, Quality, or a related field preferred.
  • Experience in pharmaceutical manufacturing, Quality Assurance, or a highly regulated environment.
  • Experience managing or coordinating cross-functional Quality projects.
  • Working knowledge of Quality Systems and regulatory compliance.
  • Familiarity with aseptic processing and/or combination products.
  • Strong analytical, organizational, and project management skills.
  • Excellent communication and interpersonal skills.
  • Ability to identify risks, develop mitigation strategies, and drive projects to completion.


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.