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Qc Analyst Ii Jobs (NOW HIRING)

Lonza

QC Analyst II, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

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

Firstsource

Quality Control Analyst II

$24.50 - $33/hr

... Quality Control function in the mortgage banking industry * Experience in quality assurance ... Analyze calculations and verifications of income & assets, and evaluations of credit reports ...

GeneFab

Quality Control Analyst I/II

Alameda, CA · On-site

$35 - $45/hr

GeneFab is seeking a Quality Control Analyst I/II to help ensure consistent quality of our cell manufacturing process. You will perform laboratory tests on incoming raw materials, in-process samples ...

Arixa Capital

QC Analyst

Los Angeles, CA · On-site

$25.75 - $34.75/hr

... $2.5 billion as of March 31, 2026. We're more than a lender. Our vertically integrated platform ... The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and ...

Arixa Capital

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

... $2.5 billion as of March 31, 2026. We're more than a lender. Our vertically integrated platform ... The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and ...

Arixa Capital

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

... $2.5 billion as of March 31, 2026. We're more than a lender. Our vertically integrated platform ... The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and ...

Arixa Capital

QC Analyst

Phoenix, AZ · Hybrid

$23.75 - $32/hr

... $2.5 billion as of March 31, 2026. We're more than a lender. Our vertically integrated platform ... The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and ...

Matthey

Quality Control Analyst

Smithfield, PA

$24.50 - $32.75/hr

Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst,you'lljoin a world leader in platinum group metals with over 200 years of ...

Johnson Matthey

Quality Control Analyst

Smithfield, PA · On-site

$24.50 - $32.75/hr

Quality Control Analyst Job title: Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst, you'll join a world leader in platinum ...

MVT Holdings

Quality Control Analyst

El Paso, TX · On-site

$45K - $55K/yr

Join our family at MVT Warehousing (Stagecoach)! We're seeking a Quality Control Analyst in El Paso ... Two years or more years' experience in warehouse, distribution, or logistics. * Experience in high ...

Corvant

Quality Control Analyst

Covington, GA

$20.25 - $27.25/hr

EQUIVALENT EXPERIENCE MAY BE CONSIDERED. 2-5 YEARS OF EXPERIENCE IN QA/QC, CONSTRUCTION, OR ... EXCELLENT ANALYTICAL, ORGANIZATIONAL, AND REPORT-WRITING SKILLS. PROFICIENCY IN MICROSOFT OFFICE ...

Actalent

Quality Control Analyst

Madison, WI

$22 - $36/hr

Bachelor's degree in Microbiology or related discipline preferred. * 2+ years preferred PCR/Micro Lab experience for Associate QC Analyst. * 5+ years preferred molecular pharmaceutical experience for ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Job Title: QC Analyst Location: Novato, CA Type: Contract Compensation: $28.00 - $32.00 Work Model: Onsite - onsite Hours: Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview ...

Ubertal Inc

Quality Control Analyst

Holly Springs, NC · On-site

$20.75 - $28/hr

Quality Control Analyst Location: Holly Springs, Wake County, North Carolina Job Type: Contract Duration: 12 months * Responsibilities: * Perform raw material compendia chemistry testing for QC ...

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How much do qc analyst ii jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for qc analyst ii 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.

Is QC analyst a stressful job?

A QC Analyst II role involves inspecting and testing products to ensure quality standards are met, which can be demanding due to strict deadlines and attention to detail. The job may involve repetitive tasks and working in regulated environments, but stress levels vary based on workload, company culture, and individual skills. Proper training and organization can help manage job-related stress effectively.

What are the key skills and qualifications needed to thrive as a QC Analyst II?

To thrive as a QC Analyst II, you need a strong background in analytical chemistry, laboratory techniques, and a relevant science degree such as Chemistry or Biochemistry. Familiarity with laboratory information management systems (LIMS), techniques like HPLC, GC, and experience with GMP/GLP regulations and certifications are typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for accurately analyzing data and reporting findings. These skills and qualifications are essential to ensure product quality, regulatory compliance, and efficient laboratory operations in quality control environments.

What is a QC Analyst II?

A QC Analyst II is a mid-level quality control professional responsible for conducting laboratory tests to ensure products meet established standards and specifications. They analyze samples, document results, troubleshoot issues with testing equipment, and help maintain compliance with regulatory guidelines. Typically, a QC Analyst II has more experience than an entry-level analyst and may train junior staff or assist in method validation. Their work is essential in industries like pharmaceuticals, biotechnology, and food manufacturing to ensure product safety and quality.

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

AspectQc Analyst IQc Analyst II
Required CertificationsTypically less experience, may require basic quality assurance certificationsMore experience, often requires advanced certifications like ASQ CQE or equivalent
Work EnvironmentEntry-level, supervised tasks in laboratory or manufacturing settingsMore independent, complex testing, and data analysis in similar environments
Job ResponsibilitiesPerform routine tests, document results, support quality checksAnalyze data, troubleshoot issues, oversee testing procedures
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, biotechSimilar industries, with increased responsibility and expertise

The main difference between a Qc Analyst I and a Qc Analyst II lies in experience, responsibilities, and certifications. Qc Analyst II roles typically require more expertise, independent work, and advanced certifications, reflecting a higher level of proficiency within the same industry and work environment.

How does a QC Analyst II typically collaborate with other departments in a pharmaceutical or biotech company?

As a QC Analyst II, collaboration with departments such as Quality Assurance, Manufacturing, and Research & Development is frequent and essential. You may be involved in cross-functional meetings to discuss test results, troubleshoot deviations, or help validate new methods or equipment. Effective communication and teamwork are critical, as your data and insights directly impact product release and compliance. These collaborations not only enhance your technical expertise but also provide valuable exposure to broader business processes, supporting career development.
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Infographic showing various Qc Analyst Ii job openings in the United States as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

QC Analyst II, Analytical - LSA

Lonza

Portsmouth, NH • On-site

$24.50 - $32.75/hr

Full-time

Medical, Dental, Vision, PTO

Re-posted 22 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 II, Analytical - Large Scale Allogenic Manufacturing
Location: Portsmouth, NH, USA.
Schedule: Monday - Friday, 0800 - 1700
We are seeking a laboratory professional to join our Quality organization in Portsmouth, NH, as a QC Analyst II in Analytical. Operating under general supervision, this bench-based role is responsible for executing critical cGMP release testing, analytical method transfers, and laboratory investigations across diverse biological and cell-based platforms.
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:
  • cGMP Bio-Testing Execution: Perform complex biological, immunological, and cell-based testing-specifically utilizing flow cytometry, ELISA, PCR assays, cell culture, cell counting, and biological potency testing-ensuring total compliance with internal SOPs, USP, and EP guidelines.
  • Method Transfer & Validation: Actively support analytical method transfer, verification, and validation activities to successfully onboard new client processes into the testing facility.
  • 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 Ownership: Initiate and author comprehensive Out-of-Specification (OOS) and laboratory deviation investigations, leveraging root-cause analysis tools to address non-conformances with proper 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 proper 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 & Mentorship: Lead by example by delivering hands-on, on-the-job training for junior QC personnel, reviewing data packets, and escalating critical laboratory anomalies to management as needed.
  • Laboratory Stewardship: Maintain laboratory benches, calibrate specialized analytical instrumentation, and propose workflow efficiency upgrades during process improvement events.

What we're looking for:
  • Experience: 2-4 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 actively participate in 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 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.

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