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Internship Quality Assurance Biotech Jobs (NOW HIRING)

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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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Quality Assurance Specialist

Shaker Heights, OH · On-site

$55K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... 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 ...

QA Engineer

Saint Louis, MO

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... internships, co-ops, academic research, or equivalent experience. * Strong analytical and problem ... Experience in a GMP-regulated environment including pharmaceutical, biotechnology, food, cosmetics ...

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Quality Assurance Specialist

Shaker Heights, OH · On-site

$55K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... 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 ...

QA Shop Floor Specialist II

Raritan, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

QA, Shop Floor Specialist II

Raritan, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Quality Assurance Technician

Burlington, MA

$30 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Biotechnology / Pharmaceutical Manufacturing Schedule: Full-Time, Tuesday - Saturday 8am - 4:30pm. About the Role We are seeking a detail-oriented Quality Assurance Specialist to support GMP ...

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Quality Assurance Inspector

Santa Ana, CA · On-site

$20 - $24/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Seeking a QA Inspector familiar with the biosciences field who can check incoming and outgoing ... or biotech environment. · Computer skills including Microsoft Word, Excel, and Outlook PREFERRED ...

QA, Shop Floor Specialist I/II

Raritan, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role OverviewThe QA Shop Floor Specialist is an exempt level position ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

QA/QC Inspector

Loves Park, IL

$20/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

QA/QC Inspector - Antibody Products Make an Impact in Biotech Quality & Innovation Join a dynamic and growing biotechnology team where your work directly supports the quality and integrity of ...

Showing results 21-40

Internship Quality Assurance Biotech information

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

As of Aug 14, 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 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.

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.
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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, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $45,740 per year, or $22 per hour.

Quality Assurance Specialist

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Re-posted 20 days ago


Job description

Job Title: Quality Assurance Specialist

Location: Indianapolis, IN
Duration: Long Term

Job Summary

We are seeking a detail-oriented Quality Assurance Specialist to support quality agreement management activities within a GMP-regulated pharmaceutical/biotech environment. The ideal candidate will be responsible for drafting, reviewing, negotiating, and maintaining quality agreements to ensure compliance with GxP regulations and internal quality standards.

The Quality Assurance Specialist will collaborate with internal cross-functional teams and external partners to support supplier qualification, regulatory compliance, and manufacturing readiness activities.

Key Responsibilities

  • Draft, review, revise, and maintain quality agreements in alignment with internal SOPs, GxP regulations, and company quality standards
  • Manage the full lifecycle of quality agreements from initiation through negotiation, execution, renewal, and closure
  • Partner with Quality Assurance, Procurement, Legal, Regulatory, and Manufacturing teams to resolve open items and obtain required approvals
  • Coordinate with external vendors, suppliers, and business partners to negotiate agreement terms and address redline comments
  • Maintain accurate tracking of agreement status, milestones, approvals, and version history within document management systems
  • Identify, communicate, and escalate risks or delays that may impact supplier qualification, product quality, regulatory compliance, or manufacturing operations
  • Support deviation investigations, CAPA activities, and change control processes related to quality systems documentation
  • Ensure compliance with FDA, cGMP, GDP, and internal quality management system requirements
  • Assist with internal audits, supplier audits, and regulatory inspections by providing quality documentation and support
  • Participate in continuous improvement initiatives related to quality agreement processes, templates, and document workflows

Experience

  • 3–5+ years of experience in a regulated pharmaceutical, biotechnology, medical device, or life sciences environment
  • Direct experience managing quality agreements, supplier quality documentation, or GxP-controlled records
  • Strong understanding of FDA regulations, cGMP, GDP, and quality systems requirements
  • Experience with document management systems, change control, CAPA, and deviation management processes
  • Strong technical writing, communication, negotiation, and organizational skills
  • Ability to manage multiple projects and deadlines within a fast-paced regulated environment