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Full Time Quality Assurance Biotech 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 ...

Amentum

Quality Assurance Manager

Idaho Falls, ID · On-site

Project Quality Assurance Manager Full-time Quality Assurance (QA) Manager of a multi-billion-dollar nuclear facility construction project, taking day-to-day direction from the Project Manager, with ...

Amentum

Quality Assurance Manager

Idaho Falls, ID · On-site

$150K - $190K/yr

Project Quality Assurance Manager Full-time Quality Assurance (QA) Manager of a multi-billion-dollar nuclear facility construction project, taking day-to-day direction from the Project Manager, with ...

Amentum

Quality Assurance Manager

Idaho Falls, ID

$150K - $190K/yr

Project Quality Assurance Manager Full-time Quality Assurance (QA) Manager of a multi-billion-dollar nuclear facility construction project, taking day-to-day direction from the Project Manager, with ...

Pae

Quality Assurance Manager

Idaho Falls, ID

Project Quality Assurance Manager Full-time Quality Assurance (QA) Manager of a multi-billion-dollar nuclear facility construction project, taking day-to-day direction from the Project Manager, with ...

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How much do full time quality assurance biotech jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for full time quality assurance biotech in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What is the difference between Full Time Quality Assurance Biotech vs Full Time Quality Control Biotech?

AspectFull Time Quality Assurance BiotechFull Time Quality Control Biotech
Primary FocusEnsuring compliance with regulations, reviewing documentation, and implementing quality systemsTesting and inspecting products, raw materials, and processes to verify quality
Work EnvironmentDocumentation review, audits, and process validation in labs and officesLaboratory testing, sampling, and analysis in lab settings
CertificationsGMP, ISO, and industry-specific quality certificationsGMP, ISO, and laboratory testing certifications

Full Time Quality Assurance Biotech roles focus on maintaining compliance and quality systems, while Full Time Quality Control Biotech positions involve testing and verifying product quality through laboratory analysis. Both roles are essential in biotech manufacturing but differ in daily tasks and focus areas.

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

The most popular types of Quality Assurance Biotech jobs are:

What states have the most Full Time Quality Assurance Biotech jobs?

States with the most job openings for Full Time Quality Assurance Biotech jobs include:

Full Time Quality Assurance Biotech jobs near you

Quality Assurance Manager

CorDx

Alpharetta, GA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 9 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.