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Internship Quality Assurance Biotech Jobs (NOW HIRING)

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Perform a range of duties within the Pharm Sci QA group, associated with oversight and support of ...

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 ...

  • 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 ...

Head of US Quality Assurance

Pennington, NJ · On-site

$190K - $250K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... The Head of Quality Assurance (QA) is responsible for leading the US Quality Assurance organization ...

New

Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical ... This is a great opportunity for individuals looking to begin their careers in biotech, particularly ...

Quality Assurance Specialist II

Albany, NY · On-site

$67K - $83K/yr

  • Retirement

  • PTO

Quality Assurance Specialist II - Albany, NY Build your future at Curia, where our work has the ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

... biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement * Strong understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S ...

Head of Quality Assurance

Fremont, CA · On-site

$191 - $202/hr

Biotech Industry Tenure: 10+ years of progressive Quality Assurance leadership experience within a GMP-regulated biotech, pharmaceutical, or advanced biologics environment. * Modality Expertise:

The Quality Assurance Engineer is responsible for ensuring that all turnkey sanitary process ... Experience in the pharmaceutical, biotech, or food processing industry. * Hands‑on experience ...

New

Quality Assurance Specialist II

Albany, NY · On-site

$67K - $83K/yr

  • Retirement

  • PTO

Quality Assurance Specialist II - Albany, NY Build your future at Curia, where our work has the ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

Quality Assurance Manager

Chandler, AZ · On-site

$120 - $165/hr

Bachelor's degree in Pharmacy, Biotechnology, Chemistry, or related scientific discipline. * 7-10 years of experience in pharmaceutical QA or manufacturing quality assurance roles. * Knowledge of ...

New

Our client is a leading biotechnology company that combines technological expertise with world ... Quality Assurance Engineer Location: Tampa, FL - 33634 Duration: 12 months Job Type: Temporary ...

Quality Assurance Specialist II in Rensselaer, NY Build your future at Curia, where our work has ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

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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 19, 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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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.

Contractor

Re-posted 23 days ago


Job description

Company Description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description

This Quality position is considered a global role reporting into the supplier management team within PharmSci QA who is responsible for supporting the Pharmaceutical Sciences R&D organization. The colleague will assist staff in managing supply chain security and performance of external parties who provide materials for GMP manufacturing. 

Responsibilities:

Key responsibilities are expected to encompass the following:

  • Perform a range of duties within the Pharm Sci QA group, associated with oversight and support of the supplier program (and may also support the external vendor inventory management function) 
  • Support efforts to introduce enhancements to the supplier program 
  • Responsible for regular communication of quality status and escalation of supplier-related quality issues, maintaining a close working relationship with Inventory Management, PharmSci QA and other sites across the Pfizer network
Qualifications
  • Minimum BS Degree or equivalent in a scientific discipline. Knowledge of cGMP, including regulations related to supplier management programs is desirable
  • Prior quality assurance experience supporting supplier management is desirable.
  • Experience using SMS, M3, QTS, PDOCS and GDMS is desirable.
  • Solid understanding of cGMPs as they relate to assigned tasks
  • Professional demeanor exhibited through the proficient use of email and phone etiquette
  • Ability to shift priorities and tasks throughout the workday to meet business requirements
Additional Information

All your information will be kept confidential according to EEO guidelines. 

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP! I want to know more about your preferences.

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