ZipRecruiter

Log In

2

Remote Gmp Quality Assurance Jobs (NOW HIRING)

Jade Biosciences

This is a fully remote role, preferably based on the U.S. West Coast, with occasional domestic and international travel. The position reports to the Senior Director, GMP Quality Assurance. Key ...

Intertek

Remote GMP Auditor

Arlington Heights, IL · Remote

Pharmaceutical, Dietary Supplement and Cosmetic GMP Auditor - Remote Intertek, a leading provider ... We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance ...

Intertek

Remote GMP Auditor

Arlington Heights, IL · On-site +1

Pharmaceutical, Dietary Supplement and Cosmetic GMP Auditor - Remote Intertek, a leading provider ... We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance ...

System One

Quality Assurance Engineer

Mahwah, NJ · Remote

$42 - $48/hr

Hybrid - onsite and remote Responsibilities * Provide quality engineering support in quality ... Familiarity with ISO 13485, GDP, GMP concepts. * Excellent communication skills and attention to ...

System One

Quality Assurance Engineer

Mahwah, NJ · Remote

$32 - $37/hr

Hybrid - onsite and remote Overview Advance your quality engineering career with a global medical ... 13485, GDP, GMP concepts highly desirable • Excellent communication skills and attention to ...

System One

Quality Assurance Engineer

Mahwah, NJ · Remote

$32 - $37/hr

Hybrid - onsite and remote Overview Advance your quality engineering career with a global medical ... 13485, GDP, GMP concepts highly desirable • Excellent communication skills and attention to ...

Gifthealth

QA Specialist - Virtual Hub

$63K - $74K/yr

Coach teams on GMP/GDP behaviors; support training, change control, and document control ... Remote * Schedule : Full-time * May require additional availability or flexibility for audits or ...

Lorven Technologies

QA

Remote need to work in EST Contract: 6+ Months Skill Set for (QA) * Qmetry (nice to have). * Postman * SQL * Azure (Familiarity only doesn't need to be expert) * At least 3 years of functional ...

Actalent

Quality Assurance Associate

Sturtevant, WI · Remote

Provide technical support and remote troubleshooting guidance to users and customers as needed ... Understanding of Good Manufacturing Practices (GMP). * Understanding of Good Laboratory Practices ...

next page

Showing results 1-20

All JobsGmp Quality Assurance JobsRemote Gmp Quality Assurance Jobs

Remote Gmp Quality Assurance information

See salary details

$12

$23

$43

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

As of Jul 26, 2026, the average hourly pay for remote gmp 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 the difference between Remote Gmp Quality Assurance vs Remote Gmp Quality Control?

AspectRemote Gmp Quality AssuranceRemote Gmp Quality Control
Primary FocusEnsuring compliance with GMP regulations, process audits, and quality systemsTesting, inspection, and product release based on quality standards
CertificationsGMP training, quality assurance certificationsGMP training, laboratory certifications
Work EnvironmentDocument review, audits, policy development (often remote)Laboratory testing, sample analysis (may be remote or on-site)
Industry UsagePharmaceutical, biotech, and medical device companiesManufacturing, pharmaceutical labs, quality testing facilities

Remote Gmp Quality Assurance focuses on maintaining compliance through audits and documentation, while Remote Gmp Quality Control emphasizes testing and inspection of products. Both roles are essential in GMP environments but differ in their core responsibilities and work activities.

What are the key skills and qualifications needed to thrive as a Remote GMP Quality Assurance professional, and why are they important?

To thrive as a Remote GMP Quality Assurance professional, you need a solid understanding of Good Manufacturing Practices, quality management systems, and a relevant degree in life sciences or engineering. Familiarity with electronic quality management systems (eQMS), audit software, and regulatory databases is typically required, along with certifications such as ASQ Certified Quality Auditor (CQA) being advantageous. Strong attention to detail, effective communication, and the ability to work independently are essential soft skills for remote collaboration and compliance oversight. These skills and qualifications ensure product safety, regulatory compliance, and efficient quality operations in distributed or virtual environments.

What are some common challenges faced by Remote GMP Quality Assurance professionals and how can they be addressed?

Remote GMP Quality Assurance professionals often encounter challenges such as maintaining effective communication with on-site teams, ensuring timely review of documentation, and managing compliance oversight from a distance. To address these issues, it's important to use secure digital collaboration tools, establish clear protocols for document sharing and review, and schedule regular video meetings to stay connected with facility staff. Proactively building relationships and setting clear expectations with colleagues can help foster trust and ensure that quality standards are consistently met, even when working remotely.

What is a Remote GMP Quality Assurance professional?

A Remote GMP (Good Manufacturing Practice) Quality Assurance professional is responsible for ensuring that products, typically in the pharmaceutical, biotechnology, or food industries, are produced and controlled according to quality standards while working remotely. Their main duties include reviewing documentation, conducting audits, overseeing compliance with GMP regulations, and supporting continuous improvement—all from a remote location. This role requires strong attention to detail, regulatory knowledge, and the ability to communicate effectively with onsite teams to maintain product quality and safety.
More about Remote Gmp Quality Assurance jobs
What cities are hiring for Remote Gmp Quality Assurance jobs? Cities with the most Remote Gmp Quality Assurance job openings:
What are the most commonly searched types of Gmp Quality Assurance jobs? The most popular types of Gmp Quality Assurance jobs are:
What states have the most Remote Gmp Quality Assurance jobs? States with the most job openings for Remote Gmp Quality Assurance jobs include:
What job categories do people searching Remote Gmp Quality Assurance jobs look for? The top searched job categories for Remote Gmp Quality Assurance jobs are:
Remote Gmp Quality Assurance jobs near you
Infographic showing various Remote Gmp Quality Assurance job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 89% Full Time, 8% Part Time, and 2% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

Director, GMP Quality Assurance

Jade Biosciences

On-site, Remote

Full-time

Posted 23 hours ago

Job description

About Jade Biosciences
Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn.
Role Overview
The Director, GMP Quality Assurance (QA) provides QA support across Jade's product pipeline across various stages of development. This role serves as a key partner to CMC and cross-functional teams, offering QA expertise, guidance and risk-based input to support development and product quality strategies.
The role provides QA oversight of contract manufacturers (CMOs) and service providers supporting cell bank, drug substance (DS), drug product (DP), finished drug product (FDP) packaging and labeling, and product distribution, ensuring alignment with GMP requirements and Jade quality standards.
Additionally, the position coordinates day-to-day GMP quality activities for outsourced manufacturing, including the intake, routing, tracking, and timely archival of quality records such as batch disposition, deviations, CAPAs, change controls, expiry/retest extensions, and product complaints. The Director collaborates with internal and external stakeholders to support timely, compliant documentation and batch release decisions. Additionally, the role may also support other QA Leads to promote cross-program alignment, consistency in QA practices, and balanced workload distribution.
This is a fully remote role, preferably based on the U.S. West Coast, with occasional domestic and international travel. The position reports to the Senior Director, GMP Quality Assurance.
Key Responsibilities
  • Serve as the QA lead for assigned GMP-related activities including quality oversight of CDMOs, tech transfer, scale-up, manufacturing (cell bank, DS, DP, FDP), and disposition of clinical materials
  • Quality reviewer and approver for quality records such as change controls, CAPAs, deviations, temperature excursions, product complaints, expiry/retest, stability protocols/reports, master batch records, method qualifications, etc.
  • Collaborate with CMC, Supply Chain, Analytical Development and Program Management to ensure on-time delivery of products and compliance with all relevant cGMP regulations and guidelines as they pertain to manufacturing and supply operations
  • Supports archival of documents/records, quality metrics and develop/maintain QA related tracking logs
  • Work directly with operating entities (internal and CMOs) to ensure that product(s) meet all required quality standards and specifications
  • Supports management of Quality Agreements, including project coordination, cross-functional review, and approval workflows
  • Represent the Quality function in product development (CMC) teams to provide proactive quality guidance and decisions
  • Influence other functional departments to ensure that CMOs achieve and maintain the appropriate levels of GMP compliance and provide the highest level of quality services to Jade
  • Lead quality risk management activities to proactively identify, assess, and mitigate GMP-related risks across manufacturing and supply operations
  • Facilitate resolution of quality issues with internal and external parties in a timely manner
  • Coordinate communications with CMOs and internal technical product teams on quality issues
  • Review CMC sections of regulatory filings, as needed
  • Collaborate cross-functionally with CMC, Regulatory, Clinical Supply Chain, and Program Leadership teams to ensure quality is embedded across development and manufacturing activities
  • Participate in and support regulatory authority inspections and internal audits
  • Supports development/maintenance of Quality SOPs
  • Contribute to the development and maintenance of a positive team-focused company culture
  • Other duties, as assigned

Qualifications
  • Bachelor's degree and 15 years of experience or a master's degree with 12+ years of experience in scientific discipline or comparable experience
  • 10+ years of experience in GMP Quality Assurance at an operational level supporting manufacturing and quality control in a pharmaceutical or biotech environment
  • Experience with all phases of development (Ph 1-4 including commercial)
  • In-depth knowledge and full understanding of GMP FDA, EMA regulations, device and combo product related guidelines, and other ICH guidelines
  • Ability to research and interpret international GMP related regulations and guidance
  • Experience managing CDMOs
  • Experience related to managing technology transfer, scale up, and validation
  • Experience supporting regulatory authority/notified body inspections
  • Experience supporting regulatory submissions (e.g. IND, BLA) and responses to health authority queries (e.g., FDA, EMA)
  • Strategic thinker with a hands-on approach; comfortable balancing long-term planning with day-to-day execution
  • Proven experience developing strong partnerships with cross functional key stakeholders to ensure that strategic business goals are met through the sharing of knowledge and teamwork
  • Must have excellent verbal, written, interpersonal and organizational skills
  • Strong communication and influencing skills, as well as problem solving ability to evaluate quality matters and make decisions utilizing risk-based approach
  • Must be self-motivated with the ability to thrive in a fast-paced, ambiguous environment while managing competing priorities
  • Excellent computer skills with working knowledge of MS Office such as Word and Excel, Visio and Adobe Acrobat professional, and familiarity with SharePoint
  • Commitment to fostering a diverse and inclusive workplace

Position Location
This is a remote role; up to 15% travel to team and company events is required.
The anticipated salary range for candidates for this role is $210,000 - $235,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography.
As part of the I-9 verification of authorization to work in the United States, Jade Bioscience participates in E-Verify. To learn more about E-Verify please review this poster.
Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

Apply