ZipRecruiter

Log In

1

Qc Analyst Ii Jobs (NOW HIRING)

Kellton Tech

QC Analyst II

Vacaville, CA · On-site

$28/hr

Position: QC Analyst II Location: Vacaville, CA (Onsite) Pay Rate : $28/hr. on W2 Summary Under limited supervision, the QC Analyst II is responsible for performing direct materials testing in ...

AMRI

Quality Control Analyst II

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst II 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 ...

AMRI

Quality Control Analyst II

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst II 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 ...

Lonza

Quality Control Analyst II

Walkersville, MD · On-site

$70K - $81K/yr

Quality Control Analyst II Location: This position is based in our Walkersville, MD office. The typical work schedule is Monday through Friday, 8:00 AM-5:00 PM EST. What you will get: The full-time ...

Lonza

QC Analyst II-Chromatography

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Job Title: QC Analyst II-Chromatography Location: Portsmouth, NH, (On-site) As a QC Analyst II, Chromatography, you will play an important role in supporting the release of in-process and final ...

Lonza

QC Analyst II-Chromatography

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Job Title: QC Analyst II-Chromatography Location: Portsmouth, NH, (On-site) As a QC Analyst II, Chromatography, you will play an important role in supporting the release of in-process and final ...

Unicon Pharma Inc.

QC Analyst II

Vacaville, CA · On-site

$27.25 - $36.50/hr

... QC Associate II, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis ...

Nova Pneuma, Inc.

QC Analyst II

Fremont, CA · On-site

$41/hr

Works on problems of moderate scope where analysis of situations or data requires a review of a ... * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a ...

Alexza

QC Analyst II

Fremont, CA · On-site

$41/hr

Works on problems of moderate scope where analysis of situations or data requires a review of a ... * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a ...

Alexza Pharmaceuticals

QC Analyst II

Fremont, CA · On-site

$41/hr

Works on problems of moderate scope where analysis of situations or data requires a review of a ... * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a ...

Lonza

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC Analyst II in Microbial Control at our Portsmouth site, you will support the testing of in-process ...

Lonza

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC Analyst II in Microbial Control at our Portsmouth site, you will support the testing of in-process ...

Genentech

Quality Control Analyst II

South San Francisco, CA · On-site

$28.75 - $38.75/hr

As a Lab Analyst, you will join our Global Analytical Development and Quality Control team, a leader in developing and executing testing methods for our biologics pipeline. You will contribute to our ...

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 ...

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 ...

next page

Showing results 1-20

All JobsManufacturing JobsProduct Manufacturing JobsQuality Control Inspector JobsQc Analyst Ii Jobs

Qc Analyst Ii information

See salary details

$16

$27

$41

How much do qc analyst ii jobs pay per hour?

As of Aug 23, 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.

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 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.

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.

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.

Is a QC Analyst II a stressful job?

A QC Analyst II role involves reviewing and testing products or materials to ensure quality standards, 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 depending on workload, company culture, and individual coping strategies.
More about Qc Analyst Ii jobs

What cities are hiring for Qc Analyst Ii jobs?

Cities with the most Qc Analyst Ii job openings:

What states have the most Qc Analyst Ii jobs?

States with the most job openings for Qc Analyst Ii jobs include:

What job categories do people searching Qc Analyst Ii jobs look for?

The top searched job categories for Qc Analyst Ii jobs are:

Qc Analyst Ii jobs near you
Infographic showing various Qc Analyst Ii job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

QC Analyst II

Kellton Tech

Vacaville, CA • On-site

$28/hr

Contractor

Re-posted yesterday

Job description

Position: QC Analyst II
Location: Vacaville, CA (Onsite)
Pay Rate : $28/hr. on W2

Summary

Under limited supervision, the QC Analyst II is responsible for performing direct materials testing in compliance with cGMP regulations. Key responsibilities include executing laboratory testing, conducting trend analysis, reviewing documentation, supporting investigations (OOS, OOT, OOE), and providing laboratory support. The QC Analyst II collaborates with Quality Control leadership to achieve departmental and organizational goals.

Job Responsibilities

  • Perform a variety of basic to moderately complex tests and document results per GMP standards.
  • Review data and assess results against established acceptance criteria.
  • Conduct technical review of peer-generated data.
  • Evaluate data to identify trends and establish limits.
  • Identify discrepancies and support the design of quality investigations and CAPA initiatives.
  • Troubleshoot technical problems and identify system or procedural gaps.
  • Provide and receive training as required.
  • Participate in assay transfers and assay validations.
  • Perform equipment qualification and maintenance.
  • Prepare and maintain standards, controls, stocks, and cultures per procedures.
  • Ensure maintenance and compliance of operational areas.
  • Apply GMP principles consistently across operations.
  • Coordinate with internal customers to support multi-site activities.
  • Support internal and external audits and regulatory inspections.
  • Meet schedules, timelines, and deadlines; maintain 95% on-time performance.
  • Participate in and/or lead group projects and process improvements.
  • Write protocols and reports with limited supervision.
  • Perform other duties as assigned to support Quality activities.

Job Requirements

  • Education & Experience:
    • B.S./B.A. degree with 3 years of experience OR
    • Master’s degree with 1 year of experience OR
    • Equivalent combination of education and relevant experience.
    • Preferred disciplines: scientific fields within pharmaceutical or biopharmaceutical industry.
  • Skills & Competencies:
    • Strong verbal and written communication skills.
    • Ability to organize and present information effectively.
    • Knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
    • Strong reasoning, judgment, and problem-solving skills.
    • Capable of working independently and setting short-term priorities.