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Quality Control Biotechnology Jobs (NOW HIRING)

TekWissen LLC

Quality Control Scientist

Eugene, OR · On-site

$25 - $28/hr

The job opportunity below is with one of our clients specializing in biotechnology product ... Quality Control Scientist Location: Eugene OR 97402 Duration: 4 Months Job Type: Temporary ...

Legend Biotech USA, Inc.

$63K - $83K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... The QC Specialist is encouraged to work independently on routine tasks and have conceptual ...

Precigen, Inc

Manager, Quality Control

Germantown, MD · On-site

$105K - $140K/yr

... and biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and assays. * 2+ years of supervisory experience. * Advanced experience with QC testing in ...

Peregrine Team

Quality Control Analyst

Seattle, WA · On-site

$27.25 - $36.75/hr

Peregrine Team is hiring a Quality Control Analyst to support laboratory testing and ensure product quality in a biotech environment. This role is essential to maintaining compliance and product ...

Actalent

CELL CULTURE & QC ASSOCIATE

Newbury Park, CA

$25 - $35/hr

Background in biotechnology, biopharmaceutical manufacturing, or QC laboratory environments. * Familiarity with GMP, GLP, HACCP, or food safety practices and their application in laboratory or ...

TekWissen LLC

Quality Control Analyst

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

Bruker Corporation

QC Inspector

Bothell, WA · On-site

$49K - $79K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

UNAVAILABLE

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

Omeros Corp.

Director, Quality Control

Seattle, WA · On-site

Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

Bruker Corporation

QC Inspector

Bothell, WA · On-site

$49K - $79K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Minimum Education: Bachelor's degree in a related field strongly ...

Bruker

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

Omeros

Director, Quality Control

Seattle, WA · On-site

Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

Kelly Services

QC Analyst Contract

Winston Salem, NC · On-site

$28 - $35/hr

Experience working in a GMP-regulated pharmaceutical, biotech, or manufacturing environment * Working knowledge of: * cGMP * SOPs * QC testing and documentation * Environmental Monitoring * Strong ...

PSG Global Solutions

Quality Control Chemist

Sanford, NC · On-site

... biotechnology and medical devices. This means we have the resources to support you within this ... quality control specifications Set up instruments and conduct sample tests; utilize a variety of ...

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Quality Control Biotechnology information

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How much do quality control biotechnology jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality control biotechnology in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is a quality control biotechnology job?

Quality Control Biotechnology jobs involve ensuring that biotechnological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet required quality and safety standards. Professionals in this field design and perform tests, analyze data, and document results to verify that products comply with regulatory guidelines. They often work in laboratories, using specialized equipment to detect contaminants or inconsistencies. These roles are crucial for maintaining product integrity and protecting public health.

What are the key skills and qualifications needed to thrive as a quality control biotechnology professional?

To thrive as a Quality Control professional in Biotechnology, you need a solid background in biology or chemistry, attention to detail, and knowledge of regulatory standards, often supported by a relevant degree. Familiarity with laboratory equipment, analytical techniques (like HPLC, PCR), and quality management systems such as GMP or ISO 9001 is typically required. Strong problem-solving skills, teamwork, and clear communication help you excel in ensuring product integrity and compliance. These skills are crucial for maintaining high product standards, meeting regulatory requirements, and ensuring the safety and efficacy of biotechnological products.

What are typical challenges faced by professionals in quality control biotechnology, and how can they be addressed?

Professionals in Quality Control Biotechnology often encounter challenges such as maintaining compliance with stringent regulatory standards, managing tight deadlines for product release, and adapting to rapidly evolving technologies. To address these issues, staying updated on regulatory changes, implementing robust documentation practices, and participating in ongoing training are essential. Collaboration with cross-functional teams, such as Research & Development and Manufacturing, also helps ensure that quality standards are integrated throughout the production process.

What is the difference between Quality Control Biotechnology vs Quality Assurance Biotechnology?

AspectQuality Control BiotechnologyQuality Assurance Biotechnology
Primary FocusTesting and inspecting biotech products to ensure they meet standardsDeveloping and implementing processes to prevent defects and ensure quality
Work EnvironmentLaboratories, testing facilitiesOffice settings, compliance departments
CertificationsGMP, GLP, laboratory certificationsGMP, ISO, audit-related certifications

While both roles aim to ensure biotech product quality, Quality Control Biotechnology focuses on testing and inspection, whereas Quality Assurance Biotechnology emphasizes process development and compliance to prevent issues. Both are essential for product integrity in the biotech industry.

How to become a quality control biotechnology specialist?

To become a quality control biotechnology specialist, candidates typically need a bachelor's degree in biotechnology, biology, or a related field. Gaining experience with laboratory techniques, quality assurance protocols, and regulatory standards such as GMP or ISO is important, and certifications like ASQ's Certified Quality Auditor can enhance prospects. Strong attention to detail, analytical skills, and familiarity with laboratory equipment are also essential for success in this role.

What does quality control biotechnology do in biotech?

Quality Control Biotechnology professionals are responsible for testing and analyzing biological products to ensure they meet safety, quality, and regulatory standards. They perform assays, validate processes, and document results using laboratory instruments and techniques, often working under Good Manufacturing Practice (GMP) guidelines. Their work helps ensure the integrity and compliance of biotech products before they reach the market.
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Quality Control Biotechnology jobs near you
Infographic showing various Quality Control Biotechnology job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Quality Control Laboratory Analyst (Raw Materials)

Pittsburgh, PA • On-site

Krystal Biotech
Biotechnology Research and Development • 51 - 200 employees
Learn more about Krystal Biotechexternal

$23.25 - $31.25/hr

Full-time

Re-posted 9 days ago

Job description

About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Position Overview:
Krystal Biotech, Inc is seeking a highly motivated Quality Control Analyst who will be responsible for in-house raw materials and product testing for the use in the manufacture of clinical and commercial drug products.
Primary Responsibilities:
  • Perform cGMP material inspection for all materials utilized for drug product manufacturing.
  • Perform cGMP material testing for all materials needed for further use in manufacturing process.
  • Review analytical data for compliance with regulations, methods and other specifications or criteria and collaborate with management when data does not meet acceptance criteria.
  • Participate in laboratory investigations, quality event investigations, protocol and report development.
  • Initiate and update quality control documentation, such as SOPs, material monographs (specification and testing documents), and test methods.
  • Support activities for Document Control and Record Retention.
  • Implementation of USP Quality Standards and verification of USP Methods.
  • Maintain equipment in the QC Lab by performing and coordinating equipment qualification, calibration, and preventive maintenance.
  • Other duties as assigned.
Requirements and Preferred Qualifications:
  • Bachelor's degree in life sciences or equivalent.
  • Experience with pH, Osmo, Endotoxin, Appearance, customized media, cell culture, and FBS testing, preferred.
  • Demonstrated experience in laboratory environment and ability to follow SOPs.
  • A demonstrated self-starter who is highly motivated and able to address changing priorities.
  • Ability to take a proactive approach on the job with the ability to work with a dynamic team.
  • Excellent scientific writing, other written and oral communication skills are required.
  • Proficient in Microsoft Word, Excel and PowerPoint.

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.

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