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Internship Quality Assurance Biotech Jobs (NOW HIRING)

CorDx

Quality Assurance Manager

Chamblee, GA

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 ...

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 ...

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 ...

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 ...

PSC Biotech

Quality Engineer

Pomona, CA · On-site

$110K - $120K/yr

At PSC Biotech, it's about more than just a job-it's about your career and your future. Your Role ... Perform QA review and approval of validation documentation. Ensure validation documents comply with ...

PSC Biotech

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

At PSC Biotech ® , it's about more than just a job-it's about your career and your future. Your ... Accordingly, the Company prohibits discrimination against qualified employees, interns and ...

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 ...

Jj

Quality Assurance Specialist ||

Raritan, NJ · On-site

Quality Assurance Job Category: Professional All Job Posting Locations: Raritan, New Jersey, United ... Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies. Janssen Biotech, Inc., one ...

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Internship Quality Assurance Biotech information

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How much do internship quality assurance biotech jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for internship quality assurance biotech in the United States is $21.99, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $24.52 per hour, depending on experience, location, and employer.

What does an internship in quality assurance in biotech involve?

An Internship in Quality Assurance (QA) in the biotech industry typically involves assisting in the development, implementation, and monitoring of quality systems to ensure that products meet regulatory standards and company policies. Interns may help with documentation, conduct audits, participate in inspections, and review procedures for compliance with Good Manufacturing Practices (GMP). This role provides hands-on experience in quality control, process validation, and understanding regulatory requirements that are critical in biotech manufacturing. It's a valuable opportunity to learn about the importance of quality in delivering safe and effective biotechnological products.

What are the key skills and qualifications needed to thrive as an internship quality assurance biotech, and why are they important?

To thrive as an Internship Quality Assurance Biotech, you generally need a background in life sciences or biotechnology, attention to detail, and basic knowledge of quality standards such as GMP or ISO. Familiarity with laboratory information management systems (LIMS), documentation tools, and regulatory databases is often required. Strong analytical thinking, communication, and teamwork skills help interns excel in quality-focused environments. These competencies ensure accurate compliance, effective documentation, and support the integrity of biotechnological research and production processes.

What are some common challenges faced during a quality assurance internship in the biotech industry?

As a Quality Assurance intern in biotech, you may encounter challenges such as understanding complex regulatory requirements, adapting to fast-paced project timelines, and learning to use specialized documentation and quality management systems. Additionally, interns often need to quickly develop a keen attention to detail, as even minor errors can impact compliance and product safety. Collaboration with cross-functional teams, such as R&D and manufacturing, is also key, so strong communication skills are essential for success in this role.

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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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Internship Quality Assurance Biotech jobs near you
Infographic showing various Internship Quality Assurance Biotech job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $45,740 per year, or $22 per hour.

Quality Assurance Manager

CorDx

Chamblee, GA

Full-time

Medical, Retirement, PTO

Re-posted 10 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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