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Quality Control Analyst Iii Jobs (NOW HIRING)

QC Analyst 3

Winston Salem, NC

$22.25 - $29.75/hr

Position Summary The QC Analyst 3 will support various duties within the Quality Control (QC) department. This position plays a key role in ensuring the technical operations of QC, focusing on the ...

QC Analyst 3

Winston Salem, NC

$22.25 - $29.75/hr

Position SummaryThe QC Analyst 3 will support various duties within the Quality Control (QC) department. This position plays a key role in ensuring the technical operations of QC, focusing on the ...

QC Analyst III

Portsmouth, NH · On-site

$25 - $30/hr

Job Title: QC Analyst III Location: Portsmouth, NH 03801 Duration: 12 months Job Type: Temporary Position Work Type: Onsite Summary * The Quality Control Technical Transfer Analyst III / QC Analyst ...

Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control Analyst III is responsible for supporting the manufacturing ...

Quality Control Analyst III

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst III in Rensselaer, NY - Nights Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization ...

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

Job Type Full-time Description Position Summary The QC Analyst III will be responsible for analytical testing and data verification/review supporting both late-stage clinical and commercial small ...

Quality Control Analyst III

Rensselaer, NY

$23.75 - $32/hr

Quality Control Analyst III in Rensselaer, NY - Nights Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization ...

QC Analyst III

Piscataway, NJ

$24 - $32.25/hr

Description Position Summary The QC Analyst III will be responsible for analytical testing and data verification/review supporting both late-stage clinical and commercial small molecule and ...

Quality Control Analyst III

Rensselaer, NY · On-site

$23.75 - $32/hr

We are currently seeking a Quality Control Analyst II to join a growing QC team in Rensselaer, NY ... Bachelor's degree in Chemistry or a related scientific discipline * 3-5 years of experience in a ...

QC Analyst 3 - Cell Therapy

Portsmouth, NH

$24.50 - $32.75/hr

Quality Control Analyst III - Cell Therapy Portsmouth, New Hampshire, USA The actual location of this job is in Portsmouth, New Hampshire, USA. Join our Quality Control team and play a key role in ...

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Quality Control Analyst

Charlotte, NC

$22.50 - $30/hr

At least 3 years of experience providing communication, quality control, and knowledge management ... Experience in data collection, analysis, and written reports summarizing data collected. * Ability ...

Quality Control Analyst

Salt Lake City, UT · On-site

$23 - $31/hr

The QC Analyst performs quality control analysis of raw material, and finished product using USP ... Other duties as assigned Job Requirements: * 3-10 or more years of experience in a laboratory ...

Quality Control Analyst I, II or III - 12 hour Nights This is a Salary Non -Exempt Role (eligible for payment of overtime in accordance with Fair Labor Standards Act) Curia is a global contract ...

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How much do quality control analyst iii jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for quality control analyst iii in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What are some common challenges Quality Control Analyst III professionals face when balancing regulatory compliance with production deadlines?

Quality Control Analyst III professionals often navigate the challenge of ensuring rigorous adherence to regulatory standards while also supporting timely production schedules. This requires keen attention to detail and proactive communication with both production and quality assurance teams to address any discrepancies or quality issues swiftly. Staying updated on evolving regulations and maintaining comprehensive documentation are crucial to avoid compliance risks. Effective time management and prioritization help analysts meet deadlines without compromising quality or regulatory standards.

What are Quality Control Analyst III?

A Quality Control Analyst III is an experienced professional responsible for ensuring the quality and compliance of products, typically in industries such as pharmaceuticals, biotechnology, or manufacturing. They conduct complex tests and inspections, analyze samples, interpret data, and help troubleshoot quality-related issues. In addition to performing advanced laboratory procedures, they often mentor junior analysts and support process improvements to meet regulatory standards. Their work is critical to maintaining product safety, consistency, and adherence to industry regulations.

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

To thrive as a Quality Control Analyst III, you need advanced knowledge of laboratory techniques, quality assurance protocols, and a relevant science degree, often supported by several years of industry experience. Proficiency with analytical instruments (such as HPLC, GC, and spectrophotometers), data analysis software, and familiarity with regulatory standards like GMP or ISO are typically required. Attention to detail, problem-solving abilities, and strong communication skills help ensure accurate results and effective collaboration across teams. These skills and qualities are crucial for maintaining product quality, regulatory compliance, and the overall integrity of laboratory operations.

What is the difference between Quality Control Analyst Iii vs Quality Control Analyst Ii?

AspectQuality Control Analyst IiiQuality Control Analyst Ii
Required CredentialsBachelor's degree in science or related field; certifications like CQE or ASQ often preferredBachelor's degree in science or related field; certifications like CQE or ASQ may be advantageous
Work EnvironmentLaboratory and manufacturing settings, performing complex testing and analysisLaboratory and manufacturing settings, conducting routine testing and data collection
Employer & Industry UsagePharmaceutical, biotech, manufacturing industries; used for advanced quality testing rolesPharmaceutical, biotech, manufacturing industries; used for entry to mid-level quality testing roles

The main difference between a Quality Control Analyst Iii and a Quality Control Analyst Ii lies in experience and complexity of tasks. The Iii typically handles more advanced testing, data analysis, and troubleshooting, while the Ii focuses on routine testing and data collection. Both roles require similar educational backgrounds and certifications, but the Iii position often demands more expertise and responsibility.

More about Quality Control Analyst Iii jobs
What cities are hiring for Quality Control Analyst Iii jobs? Cities with the most Quality Control Analyst Iii job openings:
Infographic showing various Quality Control Analyst Iii job openings in the United States as of June 2026, with employment types broken down into 56% Full Time, and 44% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.
QC Analyst 3

$22.25 - $29.75/hr

Other

Posted 8 days ago


Job description

Position Summary
The QC Analyst 3 will support various duties within the Quality Control (QC) department. This position plays a key role in ensuring the technical operations of QC, focusing on the technical suitability of bioanalytical test methods rather than day-to-day product testing. The role includes responsibility for the analytical method lifecycle, including method transfer, validation, compendial verification, performance monitoring, and continuous improvement, as well as ensuring analytical equipment is installed and qualified. The QC Analyst will support ProKidney's pipeline, from Phase III clinical development through commercial operations.

Responsibilities

Writes and executes procedures for analytical method protocols, generating reports related to QC method transfer, validation, and verification.
May write standard operating procedures (SOPs), protocols, and/or participate in instrument qualifications and analytical system validation.
Support monitoring of analytical method performance, including assessment of analytical method system suitability requirements.
Assist with data trending and aid in compilation of trend reports utilizing statistical tools.
Work with internal departments to ensure system lifecycle document readiness and support analytical instrument qualification and system validation.
Present to cross-functional teams and effectively communicate critical analytical issues and solutions.
Familiarity with FDA and EMA guidance documents relevant to cell therapy, and compendial methods from USP and EP.
Working knowledge of quality systems requirements.
Ability to work in a fast-paced, collaborative environment, managing workload based on changing priorities.
Demonstrated leadership skills and the ability to collaborate with and effectively influence others.
Establish, revise, review, perform gap-assessment, and maintain procedures (including protocols and technical reports).
Assure laboratory procedures are compliant with current requirements and facilitate updates as needed.
Complete documentation in accordance with current Good Manufacturing Practices (cGMP).
Maintain QC lab and related systems to ensure compliance with industry standards and inspection readiness.
Support CAPA's, deviations, investigations, and OOS's, ensuring effective resolution and continuous improvement.
Other tasks as assigned.

Qualifications

Bachelor's degree or equivalent in Chemistry/Biochemistry, or a related discipline.
Minimum of 5 years of relevant professional experience, including a combination of Quality Control, Analytical Development, or Microbiology. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed.
Troubleshoot equipment and analytical testing methods.
Prior experience with analytical method validations.
Excellent technical writing skills.
Familiar with ICH quality guidelines and their application in QC laboratory environments.
Thorough understanding of industry testing requirements/standards.
Excellent time management skills; organized and able to meet company deadlines.
Ability to work and prioritize under pressure in an international environment.
Familiar with FDA and EMA guidance documents relevant to gene therapy.
Experience with Analytical Instrument Qualification and System Validation in laboratory environments.
Familiarity with compendial methods including USP and EP.


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About ProKidney

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

Winston-Salem, NC, US

Year founded

2019