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Quality Control Biology Jobs (NOW HIRING)

Abzena Inc.

QC Manager

San Diego, CA · On-site

$120K - $150K/yr

With extensive experience in developing biologics and bioconjugates, we offer a seamless service ... We are seeking a highly experienced Quality Control (QC) Manager to lead cGMP QC operations ...

Actalent

Quality Control Scientist

Madison, WI

$26 - $32/hr

Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control team ... Perform molecular biology and biochemical assays involving DNA and RNA to support release ...

New

Actalent

Quality Control Scientist

Madison, WI · On-site

$26 - $32/hr

Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control team ... Perform molecular biology and biochemical assays involving DNA and RNA to support release ...

New

WuXi Biologics

Quality Control Manager, PCT

Cranbury, NJ · On-site

$73K - $155K/yr

Strong working knowledge of QC operations for biologics, including method execution, data review, and laboratory compliance. * In-depth understanding of global regulatory requirements and guidance ...

LabPersonnel

Be Seen First

Quality Control Technician

Elgin, IL · On-site

$50K/yr

Science degree (Chemistry, Biology) 1(+) year of QC experience in an industrial chemical industry. * New Graduate in scientific field (Chemistry, biology) with Zero years of relevant experience.

Zoetis, Inc.

Quality Control Manager

Charles City, IA · On-site

Manages all Biological Quality Control Operations for the Charles City site to ensure all vaccines meet US, EU and International regulatory requirements. Advise Management of products not meeting ...

Abaxis

Quality Control Manager

Charles City, IA · On-site

Manages all Biological Quality Control Operations for the Charles City site to ensure all vaccines meet US, EU and International regulatory requirements. Advise Management of products not meeting ...

Bruker Corporation

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

The Quality Control Inspector (QCII) is primarily responsible for Quality Control inspections of all Bruker Spatial Biology incoming raw materials, components and sub-assemblies received at our ...

Bruker Corporation

QC Inspector

Bothell, WA

$41K - $66K/yr

The Quality Control Inspector (QCII) is primarily responsible for Quality Control inspections of all Bruker Spatial Biology incoming raw materials, components and sub-assemblies received at our ...

Bruker

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

The Quality Control Inspector (QCII) is primarily responsible for Quality Control inspections of all Bruker Spatial Biology incoming raw materials, components and sub-assemblies received at our ...

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Quality Control Biology information

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How much do quality control biology jobs pay per hour?

As of Jul 10, 2026, the average hourly pay for quality control biology 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 do QC scientists do?

Quality Control (QC) scientists in biology are responsible for testing and analyzing biological samples to ensure products meet quality standards and regulatory requirements. They perform experiments, use laboratory instruments, and document results to identify any deviations or contamination. Their work supports product safety, efficacy, and compliance in industries like pharmaceuticals, biotech, and food production.

What are the key skills and qualifications needed to thrive as a Quality Control Biology professional, and why are they important?

To thrive as a Quality Control Biology professional, you need a strong background in biological sciences, laboratory techniques, and data analysis, typically supported by a relevant degree in biology or a related field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and analytical instruments like HPLC and PCR is essential. Attention to detail, problem-solving abilities, and effective communication are standout soft skills in this role. These competencies ensure accurate testing, regulatory compliance, and the delivery of safe, high-quality biological products.

What does a QC specialist do in biotech?

A QC (Quality Control) specialist in biotech is responsible for testing and inspecting biological products to ensure they meet quality standards and regulatory requirements. They perform assays, analyze data, and document results using laboratory instruments and techniques, often working with GMP (Good Manufacturing Practice) protocols. Their role helps ensure product safety, efficacy, and compliance throughout the manufacturing process.

What is Quality Control Biology?

Quality Control Biology refers to the process of ensuring that biological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet established standards for safety, efficacy, and quality. Professionals in this field perform tests on biological samples to detect contaminants, verify potency, and confirm that products comply with regulatory requirements. Their work is critical in the manufacturing process to prevent the release of faulty or unsafe products. Quality Control Biologists use a variety of analytical techniques and must maintain detailed records to support compliance with industry regulations.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, microbiology, biochemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance protocols, and familiarity with regulatory standards such as GMP or ISO. Certifications like ASQ Quality Auditor can enhance job prospects, and experience with laboratory instruments and data analysis is often required.

What are some common challenges faced by professionals in Quality Control Biology, and how can they be managed?

Professionals in Quality Control Biology often face challenges such as tight deadlines for sample analysis, managing multiple testing priorities, and ensuring strict compliance with regulatory standards. Effective time management and strong organizational skills are essential to handle overlapping projects and urgent requests. Additionally, clear communication and collaboration with other departments, such as production and quality assurance, can help resolve discrepancies quickly and maintain high testing accuracy. Ongoing training and staying updated on evolving industry regulations also contribute to managing these challenges successfully.

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

AspectQuality Control BiologyQuality Assurance Biology
CertificationsTypically requires a Bachelor's degree in Biology or related fieldRequires similar degrees; certifications like ASQ may be beneficial
Work EnvironmentLaboratories, manufacturing plants, testing facilitiesQuality management departments, compliance offices
Industry UsageUsed in biotech, pharmaceutical, food industries for testing productsUsed in developing and maintaining quality systems and standards
Search & Comparison IntentFocuses on testing and product quality checksFocuses on system processes and compliance standards

While both roles involve ensuring product quality, Quality Control Biology primarily focuses on testing and inspecting biological products, whereas Quality Assurance Biology emphasizes developing and maintaining quality systems and standards within the industry.

What biology jobs pay over $100k?

In the field of biology, roles such as senior research scientist, biotech director, or regulatory affairs manager often have salaries exceeding $100,000 annually. These positions typically require advanced degrees, specialized skills, and experience in areas like molecular biology, biochemistry, or laboratory management.
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What states have the most Quality Control Biology jobs? States with the most job openings for Quality Control Biology jobs include:
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Quality Control Biology jobs near you
Infographic showing various Quality Control Biology job openings in the United States as of July 2026, with employment types broken down into 76% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 81% Physical, 1% Hybrid, and 18% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.
QC Manager

QC Manager

Abzena Inc.

San Diego, CA • On-site

$120K - $150K/yr

Full-time

Posted 18 days ago

Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
We are seeking a highly experienced Quality Control (QC) Manager to lead cGMP QC operations supporting recombinant proteins and monoclonal antibody (mAb) manufacturing within a world-class biologics CDMO environment. This role is responsible for ensuring the execution, compliance, and continuous improvement of QC testing programs supporting clinical and commercial biologics release, raw materials/in-process testing, and manages a team of qualified QC professionals. This role is highly visible and interfaces directly with Manufacturing, QA, MSAT, Regulatory Affairs, and external clients, serving as a key QC subject matter expert during audits and client meetings. This position requires strong experience in QC laboratory operations and a deep understanding of cGMP/GDP testing requirements.
Responsibilities
QC Leadership and Operational Management:
  • Lead daily operations of QC Analytical lab supporting biologics testing (mAbs, recombinant proteins, fusion proteins)
  • Oversee testing activities for:
    • Drug substance and drug product release
    • Raw materials and in-process samples
    • Reference Standard management
    • Stability studies (ICH-compliant programs)
    • Testing associated with Qualification/Validation of Test Methods
    • Ensure timely execution of testing to support manufacturing schedules and batch disposition
    • Drive training programs, scheduling, and technical capability development
    • Timely maintenance of calibration, PM, qualification of lab instruments
  • Lead daily operations of QC Analytical lab supporting biologics testing (mAbs, recombinant proteins, fusion proteins)
  • Provide leadership, mentorship, and develop QC associates (typically 4-6 + team members)
  • Communicate departmental goals, priorities, and performance expectations to direct reports
  • Drive lean laboratory practices, resource planning, and operational excellence initiatives
  • Support strategic planning for new equipment, staff capacity planning, organizational structure, and resource requirements.
  • Improve turnaround time (TAT), right-first-time execution, and lab efficiency
  • Maintain accurate and current release/stability inventory records, testing schedules, and timely issuance of associated CoA's and summary sheets.
  • Represent QC analytical in internal meetings, client meetings, audits, and cross-functional discussions related to stability and reference standards.
  • Author and/or review deviations, investigations, CAPAs, change controls, and risk assessments related to stability and reference standard programs.
  • Support or lead investigations involving OOS, OOT, non-conformances, and laboratory events.
  • Review analytical data packages, perform data trending, and provide troubleshooting support for complex laboratory issues.
  • Occasional travel may be required between Abzena sites, including San Diego, California and Bristol, Pennsylvania.

Qualifications
  • Bachelor's degree or higher in Chemistry, Biology, or related Life Sciences discipline
  • Minimum 10 years of experience in QC GMP pharmaceutical or biotechnology laboratories within a cGMP-regulated environment
  • Minimum 5-6 years of people management experience in QC laboratory settings
  • Extensive knowledge of HPLC, ELISA, Capillary Electrophoresis (CE), cIEF (Maurice platform), UV-Vis, cell-based potency assay, and compendial methods.
  • Knowledge of ICH, EP, USP, and FDA guidelines relating to method development, qualification/validation, and stability studies.

$120,000 - $150,000 a year
FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local Jaws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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