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Qc 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

$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

$24.25 - $32.50/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

$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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Qc Analyst Iii information

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$41

How much do qc analyst iii jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for qc 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 QC Analyst III?

A QC Analyst III is an experienced quality control professional responsible for testing, analyzing, and ensuring the quality of products, typically in industries like pharmaceuticals, biotechnology, or food manufacturing. They perform advanced laboratory tests, interpret data, and ensure compliance with regulatory standards. In addition to their technical duties, QC Analyst IIIs may also train junior analysts, help develop testing protocols, and participate in investigations of quality issues.

What are some common challenges faced by a QC Analyst III when working with cross-functional teams?

As a QC Analyst III, one common challenge when collaborating with cross-functional teams is ensuring clear communication and alignment on testing protocols and timelines, especially when priorities shift quickly. QC Analysts at this level often serve as a technical resource, which means they must translate complex analytical findings to non-technical colleagues in manufacturing, R&D, or regulatory affairs. Balancing multiple projects and managing expectations while upholding quality standards can also be demanding, but these interactions provide valuable opportunities to influence decision-making and drive process improvements.

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

To thrive as a QC Analyst III, you need advanced knowledge of analytical chemistry, laboratory techniques, and quality control standards, often supported by a relevant science degree and substantial industry experience. Familiarity with laboratory information management systems (LIMS), chromatographic software (such as HPLC or GC), and regulatory compliance (GMP/GLP) is typically required. Strong attention to detail, problem-solving skills, and effective communication are crucial soft skills for this role. These skills and qualities ensure accurate data analysis, compliance with regulations, and maintenance of product quality and safety.

What is the difference between Qc Analyst Iii vs Qc Analyst Ii?

AspectQc Analyst IiiQc Analyst Ii
Required CredentialsBachelor's degree in life sciences or related field; relevant certifications (e.g., ASQ)Bachelor's degree; some certifications preferred
Work EnvironmentLaboratory setting, quality control labs in pharma/biotechLaboratory environment, similar industry
Job ResponsibilitiesComplex testing, data analysis, mentoring junior staffRoutine testing, data recording, basic troubleshooting
Experience LevelTypically 3+ years1-3 years

The main difference between Qc Analyst Iii and Qc Analyst Ii lies in experience, responsibilities, and complexity of tasks. Qc Analyst Iii generally handles more complex testing, provides mentorship, and requires more experience and certifications, whereas Qc Analyst Ii focuses on routine testing and data recording with less seniority.

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Qc Analyst Iii jobs near you
Infographic showing various Qc Analyst Iii job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 88% Full Time, 6% Part Time, 1% Temporary, and 4% Contract. Highlights an 80% Physical, 7% Hybrid, and 13% 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 18 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

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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