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Internship Quality Assurance Biotech Jobs (NOW HIRING)

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 ...

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

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 ...

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 ...

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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 Aug 28, 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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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 86% Full Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $45,740 per year, or $22 per hour.

Quality Assurance Engineer

Rochester, NY • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 28 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Quality Assurance Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Quality Assurance Engineer
Location: New York
Duration: Long Term

Position Overview

We are seeking an experienced Quality Assurance Engineer to support quality assurance activities within a pharmaceutical, biotechnology, or medical device manufacturing environment. This role will focus on ensuring product quality, regulatory compliance, and continuous process improvement by supporting quality systems, inspections, audits, documentation, and CAPA activities. The ideal candidate will have strong knowledge of FDA regulations, GMP, ISO standards, and quality management systems while collaborating with cross-functional teams to maintain the highest quality standards.

Key Responsibilities

• Perform quality inspections, manufacturing audits, and process reviews to ensure compliance with quality standards.

• Review batch records, device history records, and quality documentation for accuracy and regulatory compliance.

• Ensure compliance with FDA regulations, GMP, ISO 13485, and company quality management systems.

• Investigate quality issues, non-conformances, deviations, and customer complaints, and support CAPA activities.

• Participate in internal audits, supplier audits, and regulatory inspections while ensuring audit readiness.

• Collaborate with Manufacturing, Engineering, Regulatory Affairs, Validation, and Quality Control teams to improve product quality and manufacturing processes.

• Develop, review, and maintain quality procedures, SOPs, work instructions, and technical documentation.

• Support risk assessments, root cause analysis, change control, and continuous improvement initiatives.

• Monitor quality metrics and analyze trends to identify opportunities for process improvement and operational excellence.

• Ensure compliance with company quality policies and applicable regulatory requirements throughout the product lifecycle.

Required Qualifications

• Bachelor's Degree in Engineering, Biotechnology, Life Sciences, Chemistry, Biology, or a related scientific discipline.

• 2–5 years of Quality Assurance experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.

• Strong knowledge of FDA regulations, GMP, ISO 13485, CAPA, Quality Management Systems (QMS), and regulatory compliance requirements.

• Experience performing quality inspections, manufacturing audits, documentation review, and quality investigations.

• Hands-on experience with deviations, non-conformances, root cause analysis, CAPA, and change control processes.

• Familiarity with quality documentation, batch record review, SOP development, and document control systems.

• Experience supporting internal audits, supplier audits, and regulatory inspections.

• Strong analytical, problem-solving, technical documentation, and organizational skills.

• Excellent communication and cross-functional collaboration skills with the ability to work effectively in a regulated environment.

• Experience working within pharmaceutical, biotechnology, or medical device manufacturing facilities is highly preferred.

• Knowledge of statistical quality tools, risk management methodologies, Lean Manufacturing, or Six Sigma is an added advantage.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/