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From Home Quality Assurance Biotech Jobs (NOW HIRING)

Krystal Biotech

Quality Assurance Associate

Moon, VA · On-site

$60 - $80/hr

About Krystal Bio At Krystal Biotech, we bring together the brightest and most eager minds to ... Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP ...

Krystal Biotech

$60 - $80/hr

At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the ... Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP ...

Legend Biotech US

Director, QA Operations

Raritan, NJ · On-site

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... From our global network of research and development sites, we are committed to discovering and ...

Calvary Healthcare

Quality Assurance RN

Bronx, NY · On-site

For over 125 years, Calvary Hospital and Calvary @Home located in the Bronx, New York has been ... The hospice receives patients from referring institutions throughout New York City and the entire ...

Calvary Hospital

Quality Assurance RN

Bronx, NY

For over 125 years, Calvary Hospital and Calvary @Home located in the Bronx, New York has been ... The hospice receives patients from referring institutions throughout New York City and the entire ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

Aspect Biosystems

Head of Quality Assurance

Fremont, CA · On-site

$191K - $202K/yr

... the entire product value chain, from early development through clinical manufacturing ... Biotech Industry Tenure: 10+ years of progressive Quality Assurance leadership experience within a ...

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How much do from home quality assurance biotech jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for from home quality assurance biotech in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $25.72 per hour, depending on experience, location, and employer.

What is a from home quality assurance biotech job?

From Home Quality Assurance Biotech jobs involve overseeing and ensuring the quality and compliance of biotech products and processes while working remotely. These professionals review documentation, perform virtual audits, monitor data integrity, and ensure that all products and procedures meet regulatory standards such as FDA or ISO requirements. They typically collaborate with laboratory teams, regulatory bodies, and management through digital platforms, making strong communication and analytical skills essential. Remote QA roles in biotech are increasingly common, allowing for flexibility while maintaining rigorous quality standards.

What are the key skills and qualifications needed to thrive as a from home quality assurance biotech professional?

To thrive as a Work-from-Home Quality Assurance Biotech professional, you need a strong background in life sciences, experience with QA processes, and familiarity with regulatory standards such as GMP or GLP. Proficiency with digital QA tools, laboratory information management systems (LIMS), and relevant certifications like ASQ Certified Quality Auditor are commonly required. Outstanding attention to detail, problem-solving abilities, and effective remote communication skills set top performers apart. These competencies ensure compliance, data integrity, and product safety in biotech operations, even when working remotely.

What types of communication and collaboration tools are commonly used by remote quality assurance professionals in biotech companies?

Remote Quality Assurance (QA) professionals in biotech typically rely on a mix of collaboration platforms such as Microsoft Teams, Slack, or Zoom for real-time communication with team members and stakeholders. Additionally, project management and documentation tools like Jira, Confluence, and electronic quality management systems (eQMS) are frequently used to track progress, manage audits, and ensure compliance. Effective use of these tools is essential for maintaining clear documentation and seamless teamwork, especially when coordinating with cross-functional teams such as regulatory affairs, manufacturing, and R&D. Proficiency with digital collaboration platforms is highly valued and helps ensure quality standards are consistently met, even in a remote work environment.

What is the difference between From Home Quality Assurance Biotech vs From Home Quality Control Biotech?

AspectFrom Home Quality Assurance BiotechFrom Home Quality Control Biotech
Primary FocusEnsuring compliance, process audits, and documentation accuracyTesting, analyzing, and verifying product quality and specifications
CertificationsGMP, ISO, QA certifications often requiredLab certifications, technical testing certifications
Work EnvironmentRemote, documentation-heavy, regulatory-focusedRemote or lab-based, testing and analysis tasks
Industry UsageCommon in biotech, pharmaceutical, and healthcare companiesCommon in biotech, pharmaceutical, and manufacturing sectors

While both roles support biotech companies, From Home Quality Assurance Biotech focuses on compliance, audits, and documentation to ensure regulatory standards are met. In contrast, From Home Quality Control Biotech emphasizes testing and verifying product quality through laboratory analysis. Both roles require relevant certifications and are integral to maintaining product integrity in the biotech industry.

What cities are hiring for From Home Quality Assurance Biotech jobs?

Cities with the most From Home Quality Assurance Biotech job openings:

What are the most commonly searched types of Quality Assurance Biotech jobs?

The most popular types of Quality Assurance Biotech jobs are:

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States with the most job openings for From Home Quality Assurance Biotech jobs include:

From Home Quality Assurance Biotech jobs near you

Quality Assurance Associate

Krystal Biotech

Pittsburgh, PA • On-site

Full-time

Re-posted 10 days ago

Job description

About Krystal Bio:
At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Job Description Summary:
Krystal Biotech, Inc. is seeking a highly motivated and experienced Quality Associate to support quality systems, GMP manufacturing processes and documentation practices at our headquarters in Pittsburgh's South Side.
Primary Responsibilities:
  • Work with internal teams to obtain an understanding of the product and the documentation requirements.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended use.
  • Develop expertise on FDA regulations and audit processes.
  • Initiate and update GMP manufacturing associated documentation, such as clearing procedures.
  • Provide oversight of daily QA functions which include review and approval of records generated by manufacturing and quality control documents.
  • Provide support for updates on standard operating procedures and associated forms.
  • Assist with QA efforts for site cGXP documentation related to the operation of gene therapy manufacturing.
  • Ensure compliance with regulatory agencies and oversee continuous improvement of company's QA and compliance functions.
Requirements & Desired Competencies:
  • Minimum of a Bachelor's Degree (Biology or related Life Science) with 3+ years of relevant quality systems experience in the biotech or pharmaceutical industry.
  • Background that includes knowledge/experience in GMP, GLP, and GCP.
  • Experience with FDA audits is highly preferred.
  • Strong knowledge of GMP and ICH requirements.
  • Must be a self-starter and capable of working with minimal oversight.
  • Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately.
  • Excellent oral and written communication skills.

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.
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