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Temporary 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 ...

CorDx

Quality Assurance Manager

Alpharetta, 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 ...

Trulieve

Quality Assurance Technician

Quincy, FL · On-site

Quincy, FL POSITION SUMMARY The Temporary - Quality Assurance Technician - Processing is responsible for conducting visual scans of products to assure the quality and safety profiles of products ...

CorDx

Quality Assurance Manager

Chamblee, 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 ...

Legend Biotech USA, Inc.

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role OverviewThe QA Investigation Lead is an exempt level position reporting to the QA ...

Cellular Technology Limited (CTL)

Be Seen First

Quality Assurance Specialist

Shaker Heights, OH · On-site

$55K - $70K/yr

... a global biotechnology company with locations and distributors worldwide. We are the industry ... As the Quality Assurance Specialist, you will support and contribute to the Quality Management ...

Cellular Technology Limited (CTL)

Be Seen First

Quality Assurance Specialist

Shaker Heights, OH · On-site

$55K - $70K/yr

... a global biotechnology company with locations and distributors worldwide. We are the industry ... As the Quality Assurance Specialist, you will support and contribute to the Quality Management ...

Legend Biotech USA, Inc.

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the floor ...

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Temporary Quality Assurance Biotech information

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

As of Aug 8, 2026, the average hourly pay for temporary 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 Temporary Quality Assurance Biotech vs Temporary Quality Control Biotech?

AspectTemporary Quality Assurance BiotechTemporary Quality Control Biotech
CertificationsGMP, GLP, QA certificationsGMP, GLP, QC certifications
Work EnvironmentDocumentation review, audits, complianceTesting, lab analysis, sample testing
Employer & Industry UsagePharmaceutical, biotech companies, manufacturingLaboratories, manufacturing, biotech firms

Temporary Quality Assurance Biotech focuses on ensuring compliance, documentation, and audit readiness, while Temporary Quality Control Biotech emphasizes testing, analyzing samples, and product quality verification. Both roles are essential in biotech manufacturing but differ in daily tasks and focus areas.

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

To thrive as a Temporary Quality Assurance Biotech, you need a background in biological sciences or a related field, strong attention to detail, and an understanding of regulatory standards like GMP or GLP. Familiarity with laboratory information management systems (LIMS), quality management software, and relevant certifications such as ASQ are highly beneficial. Excellent organizational skills, clear communication, and the ability to work well in a team help ensure seamless compliance and reporting. These skills and qualities are crucial to maintaining product quality, regulatory compliance, and efficient operations in a biotech environment.

What is a temporary quality assurance biotech?

Temporary Quality Assurance Biotech jobs involve short-term roles in biotechnology companies where professionals ensure that products and processes meet established quality standards and regulatory requirements. These positions typically focus on tasks such as monitoring laboratory practices, conducting audits, reviewing documentation, and supporting compliance efforts. Individuals in these roles help maintain product safety and efficacy by identifying issues and implementing corrective actions. Temporary QA positions are often used to support peak workloads, special projects, or to cover employee absences.

What are some typical challenges faced by temporary quality assurance biotech professionals, and how can they overcome them?

Temporary Quality Assurance (QA) professionals in biotech often encounter challenges such as quickly adapting to new protocols, integrating into established teams, and rapidly learning complex regulatory requirements. Since their assignments are time-bound, it's crucial to familiarize themselves with company-specific quality systems and documentation processes early on. Proactively seeking guidance from permanent team members and leveraging available training resources can help temporary QA staff contribute effectively and ensure compliance with industry standards.
What cities are hiring for Temporary Quality Assurance Biotech jobs? Cities with the most Temporary 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:
What states have the most Temporary Quality Assurance Biotech jobs? States with the most job openings for Temporary Quality Assurance Biotech jobs include:
Temporary Quality Assurance Biotech jobs near you

Quality Assurance Manager

CorDx

Alpharetta, GA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 12 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.