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Biotech Qa Jobs (NOW HIRING)

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 ...

Danaher

Quality Assurance (QA) Specialist

Boulder, CO · On-site

$63K - $80K/yr

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... The Quality Assurance (QA) Specialist is responsible for providing administration, coordination ...

Madrigal Pharmaceuticals

Experience in pharmaceutical / biotech Quality Systems, global standards deployment, lifecycle management across Development QA to Commercial QA, and operating effectively within a virtual biotech ...

Aspect Biosystems

Head of Quality Assurance

Fremont, CA · On-site

$191K - $202K/yr

Biotech Industry Tenure: 10+ years of progressive Quality Assurance leadership experience within a GMP-regulated biotech, pharmaceutical, or advanced biologics environment. * Modality Expertise:

Legend Biotech USA, Inc.

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the floor ...

Danaher

Quality Assurance (QA) Specialist

Boulder, CO · On-site

$63K - $80K/yr

... biotechnology? AtIntegrated DNA Technologies (IDT),one ofDanaher's15+ operating companies, our work ... The Quality Assurance (QA) Specialist is responsibleforproviding administration, coordination, and ...

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Biotech Qa information

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$10

$46

$73

How much do biotech qa jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for biotech qa in the United States is $46.70, according to ZipRecruiter salary data. Most workers in this role earn between $29.81 and $62.02 per hour, depending on experience, location, and employer.

What is a Biotech QA?

Biotech QA (Quality Assurance) professionals are responsible for ensuring that products developed in the biotechnology industry meet regulatory standards and quality requirements. They oversee processes to ensure compliance with Good Manufacturing Practices (GMP), conduct audits, review documentation, and collaborate with other departments to maintain product integrity. QA professionals play a critical role in preventing errors, ensuring safety, and facilitating the approval of biotech products by regulatory agencies like the FDA. Their work helps protect consumers and supports the successful commercialization of new biotechnological innovations.

What are the key skills and qualifications needed to thrive as a Biotech QA?

To thrive as a Biotech QA, you need a strong background in life sciences, quality assurance processes, and regulatory compliance, often supported by a relevant degree and experience in biotech or pharmaceuticals. Familiarity with quality management systems (QMS), Good Manufacturing Practices (GMP), and tools like LIMS or CAPA systems is typically required, with certifications such as ASQ CQE being advantageous. Strong attention to detail, problem-solving abilities, and effective communication skills are essential soft skills for this role. These competencies ensure that biotech products meet stringent regulatory standards and maintain high quality, safeguarding consumer safety and company reputation.

What are some common challenges faced by Biotech QA professionals when ensuring compliance with industry regulations?

Biotech QA professionals often encounter challenges such as staying up-to-date with evolving regulatory requirements, managing complex documentation, and ensuring consistency across multiple teams and processes. They must balance strict compliance with the need for efficiency in dynamic research and production environments. Collaborating with scientists, engineers, and production staff, QA professionals play a crucial role in identifying potential risks, conducting audits, and implementing corrective actions to maintain product quality and regulatory standards.

What is the difference between Biotech Qa vs Biotech Quality Control Analyst?

AspectBiotech QaBiotech Quality Control Analyst
CredentialsBachelor's in Life Sciences, Quality Certifications (e.g., ASQ)Bachelor's in Life Sciences, Quality Certifications (e.g., ASQ)
Work EnvironmentQuality assurance departments, documentation review, auditsLaboratory testing, sample analysis, data recording
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract labsBiotech and pharmaceutical manufacturing, testing labs

Biotech Qa professionals focus on ensuring overall quality systems, audits, and compliance, while Biotech Quality Control Analysts primarily perform laboratory testing and sample analysis. Both roles require similar credentials and work within biotech environments, but their daily tasks and focus areas differ.

What cities are hiring for Biotech Qa jobs?

Cities with the most Biotech Qa job openings:

What states have the most Biotech Qa jobs?

States with the most job openings for Biotech Qa jobs include:

What are popular job titles related to Biotech Qa jobs?

For Biotech Qa jobs, the most frequently searched job titles are:

Biotech Qa jobs near you
Infographic showing various Biotech Qa job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 89% Full Time, 4% Part Time, 5% Contract, and 1% Nights. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $97,144 per year, or $46.7 per hour.

Quality Assurance Manager

Alpharetta, GA • On-site

CorDx
Biotechnology Research and Development • 1 - 5K employees
Learn more about CorDxexternal

Full-time

Medical, Retirement, PTO

Re-posted 21 days ago

Job description

Who is CorDx?
CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.
Position: QA Manager
Location: Alpharetta/Chamblee
Position Type: 5 days Onsite Exempt Position
Job Summary: We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the development, manufacturing, and distribution of Class II IVD devices. The ideal candidate will have at least 7 years of experience in the IVD industry, with a strong background in quality management systems, regulatory compliance, and team leadership.
Key Responsibilities:
Quality Systems & Compliance
  • Develop, implement, and maintain Quality Management Systems (QMS) in accordance with, US FDA, ISO 13485, and applicable regulations.
  • Lead internal and external audits, regulatory inspections, and corrective action plans (CAPAs).
  • Oversee batch record reviews, deviations, non-conformance reports (NCRs), and change controls to maintain product quality and integrity.

Process & Product Quality Assurance
  • Develop and enforce Standard Operating Procedures (SOPs) and best practices to ensure consistent quality across manufacturing operations.
  • Collaborate with R&D, production, and regulatory affairs teams to ensure new products and processes meet quality standards.
  • Monitor and analyze quality metrics (KPIs) to drive continuous improvement initiatives.
  • Ensure adherence to Good Documentation Practices (GDP) and data integrity policies.

Leadership & Team Development
  • Lead, mentor, and develop the QA team, fostering a culture of quality, compliance, and continuous improvement.
  • Train manufacturing and quality teams on quality systems, and root cause analysis (RCA) methodologies.
  • Serve as the primary point of contact for quality-related issues and escalations.

Risk Management & Continuous Improvement
  • Identify quality risks and implement proactive mitigation strategies.
  • Lead investigations and root cause analyses for product defects, deviations, and non-conformances.
  • Drive LEAN, Six Sigma, or other process improvement initiatives to enhance efficiency and reduce waste.
  • Stay updated on industry trends, new regulations, and technological advancements in medical device IVD quality assurance.

Requirements
  • Bachelor's or Master's degree in Biotechnology, Microbiology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
  • 7+ years of experience in quality assurance within biotech, pharmaceutical, or medical device manufacturing.
  • 3+ years in a managerial or leadership role overseeing QA teams.

  • Skills & Competencies
  • Strong knowledge of US FDA, ISO 13485, and other regulatory standards.
  • Experience with QA audits, inspections, CAPA investigations, and risk management.
  • Proficiency in QMS software and documentation control systems.
  • Strong analytical and problem-solving skills, with a data-driven approach to decision-making.
  • Excellent leadership, communication, and cross-functional collaboration skills.

Benefits
  • Medical Insurance Plan
  • Retirement Plan
  • Paid Time Off
  • Training & Development
    We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.

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