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Quality Control Analyst Iii Jobs (NOW HIRING)

Lonza

QC Analyst III, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA. Schedule: Monday - Friday, 8:00 AM-5:00 PM We are seeking an advanced laboratory professional to join ...

Lonza

QC Analyst III, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA. Schedule: Monday - Friday, 0800-1700 We are seeking an advanced laboratory professional to join our ...

Fred Hutch

Quality Control Analyst III/IV

Seattle, WA · On-site

$27.25 - $36.75/hr

Quality Control Analyst III: * BS/MS in a biological science or equivalent level of expereince. * Minimum 5 years (2+ years MS) with a background in biologics and/or cellular therapeutics.

Lonza

QC Analyst III, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA. Schedule: Monday - Friday, 0800-1700 We are seeking an advanced laboratory professional to join our ...

Sub-Zero, Inc.

SAP QC Analyst III

Madison, WI · On-site

$80 - $100/hr

SAP QC Analyst III must be detail oriented, have strong analytical and problem solving abilities. Must understand and conceptualize applications from both a technical/programming perspective and a ...

Sub-Zero Group, Inc.

SAP QC Analyst III

Madison, WI · On-site

$24.25 - $32.50/hr

The SAP QC Analyst III must be detail oriented, have strong analytical and problem solving abilities. Must understand and conceptualize applications from both a technical/programming perspective and ...

Sub-Zero & Wolf Appliance

SAP QC Analyst III

Madison, WI · On-site

$24.25 - $32.50/hr

The SAP QC Analyst III must be detail oriented, have strong analytical and problem solving abilities. Must understand and conceptualize applications from both a technical/programming perspective and ...

ProSidian Consulting

Quality Control Analyst

Charlotte, NC · On-site

$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 ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

... Analyst ... Ideal candidates should have a bachelors degree and 0-3 years of relevant laboratory experience; QC ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

... Analyst ... Ideal candidates should have a bachelors degree and 0-3 years of relevant laboratory experience; QC ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

... Analyst ... Ideal candidates should have a bachelors degree and 0-3 years of relevant laboratory experience; QC ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

... Analyst ... Ideal candidates should have a bachelors degree and 0-3 years of relevant laboratory experience; QC ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

... Analyst ... Ideal candidates should have a bachelors degree and 0-3 years of relevant laboratory experience; QC ...

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Quality Control Analyst Iii information

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

As of Sep 9, 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 is a 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?

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 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 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.

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Quality Control Analyst Iii jobs near you
Infographic showing various Quality Control Analyst Iii 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 $58,065 per year, or $27.9 per hour.

QC Analyst III, Analytical - LSA

Portsmouth, NH • On-site

Lonza
Biotechnology Research and Development • 10K+ employees
Learn more about Lonzaexternal

$24.50 - $32.75/hr

Full-time

Medical, Dental, Vision, PTO

Re-posted 15 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing
Location: Portsmouth, NH, USA.
Schedule: Monday - Friday, 8:00 AM-5:00 PM
We are seeking an advanced laboratory professional to join our Quality organization in Portsmouth, NH, as an Analyst III, QC Analytical. Operating under general supervision, this senior bench-based role executes critical cGMP release testing, handles method validation protocols, and drives complex laboratory investigations.
What will you get?
  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Compensation programs that recognize high performance
  • Medical, dental and vision insurance, as well as PTO and more
  • Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you'll do:
  • Advanced cGMP Release Testing: Execute complex biological, immunological, and cell-based testing-specifically utilizing flow cytometry, ELISA, PCR assays, cell culture, and cell counting-ensuring total compliance with internal SOPs, USP, and EP guidelines to support on-time in-process control and final product release.
  • Assay Transfer & Method Validation: Actively spearhead analytical method transfers, qualifications, and validation protocols, including onboarding new methodologies and configuring advanced laboratory instrumentation.
  • Data Review & Verification: Review raw laboratory records, data calculations, and execution logs for absolute accuracy, protocol compliance, and strict adherence to Good Documentation Practices (GDP).
  • Investigation & OOS Ownership: Lead comprehensive Out-of-Specification (OOS) and laboratory deviation investigations, leveraging root-cause analysis tools to address complex non-conformances with minimal support.
  • CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions (CAPAs) and detail structured Change Controls to promote compliance and continuous laboratory improvement with minimal support.
  • Document Architecture: Develop, modify, and sustain standard operating procedures (SOPs), master forms, and test records to match evolving industry expectations and site improvements.
  • Peer Training & Floor Leadership: Deliver hands-on, on-the-job training for junior QC personnel, reviewing data packets, modeling strong work ethics, and escalating critical laboratory anomalies to management as needed.

What we're looking for:
  • Experience: 3-4+ years of direct Quality Control laboratory experience within a cGMP biomanufacturing or regulated clinical testing setting is required.
  • Technical Mastery: Proven, hands-on experience performing cell culture maintenance, immunophenotyping panels via flow cytometry, PCR amplification, and standard immunological assay techniques.
  • Systems & Digital Compliance: Familiarity with Laboratory Information Management Systems (LIMS), enterprise data management applications, and quality systems software (such as TrackWise) is highly preferred.
  • Investigation Savvy: Demonstrated ability to independently lead laboratory event investigations, formulate root-cause theories, and write clear, logical technical summaries.
  • Education: Bachelor's Degree in Biochemistry, Biology, or a closely related technical science discipline is required. A Master's Degree in a scientific discipline is preferred.
  • Soft Skills: Superior written and oral communication skills, a solutions-focused team attitude, and the personal initiative required to navigate multiple testing demands and overcome performance roadblocks without routine reminders.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

What Lonza employees say

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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