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Quality Control Associate Ii Jobs (NOW HIRING)

Fladger Associates

QC Associate

Fremont, CA · On-site

Excellent employment opportunity for a QC Associate III in the Fremont, CA area. * Performs sampling/testing/inspection of raw materials, conducts lab investigations, and reports aberrant results to ...

The Rizzo Companies

QA/QC Associate

Danbury, CT · On-site

Quality Assurance/Quality Control Associate Position Summary Rizzo Corporation is seeking a ... Minimum of 2-3 years of construction, inspection, or quality control experience. OSHA 10 or 30 ...

The Rizzo Companies

QA/QC Associate

Danbury, CT · On-site

Quality Assurance/Quality Control Associate Position Summary Rizzo Corporation is seeking a ... 2-3 years of construction, inspection, or quality control experience. • OSHA 10 or 30 ...

Fanatics Collectibles

QC Associate

Allen, TX · On-site

... 2,500 athletes and celebrities, and 200 exclusive athletes; and over 2,000 retail locations ... Role Summary The QC Associate ensures the highest standards of quality in the production of trading ...

System One

Quality Control Associate

Oro Valley, AZ · On-site

$25.75/hr

Quality Control Associate Location: Oro Valley, AZ Type: Contract Compensation: $25.75/hr Work Model: Onsite Hours: M-F normal business hours Security Clearance: Not specified Overview Leave ...

CYNET SYSTEMS

Quality Control Associate

Tucson, AZ · On-site

$25/hr

... Associate's Degree. * Less than 1 year work experience, entry level with a Bachelor's Degree ... Maintain records and QC lab environment to comply with cGMP, OP and regulatory requirements.

UA Brands

Quality Control Associate

Lithia Springs, GA · On-site

As a Quality Control Associate, Execute planned quality control inspections on goods in adherence ... Earn $2.00 more/hour for weekend shifts * Must be able to work Saturdays and Sundays, as needed ...

Onin Staffing

Quality Control Associate

Meridian, MS

$15 - $16/hr

We are seeking a detail-oriented and dependable Quality Control Associate to inspect products and materials to ensure they meet established quality standards. The ideal candidate will have strong ...

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Quality Control Associate Ii information

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How much do quality control associate ii jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for quality control associate ii in the United States is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.01 per hour, depending on experience, location, and employer.

What is a quality control associate ii?

Quality Control Associate IIs are professionals responsible for performing intermediate-level testing and inspections in laboratories or manufacturing environments to ensure products meet established quality standards. They analyze samples, document test results, and help maintain compliance with regulatory requirements. These associates may also assist in troubleshooting issues, calibrating equipment, and training junior staff. Typically, they report to Quality Control Supervisors or Managers and play a key role in ensuring product safety and reliability.

What skills and qualifications are needed to be a quality control associate ii?

To thrive as a Quality Control Associate II, you generally need a background in life sciences or chemistry, experience with laboratory testing, and knowledge of GMP or GLP regulations. Familiarity with analytical instruments such as HPLC, GC, and LIMS software, as well as relevant certifications, is typically required. Strong attention to detail, analytical thinking, and effective communication are standout soft skills in this position. These skills and qualifications are essential for ensuring product quality, regulatory compliance, and the reliability of laboratory results.

What are common challenges faced by a quality control associate ii, and how can they be addressed?

Quality Control Associate II professionals often encounter challenges such as managing tight deadlines for testing and documentation, adapting to evolving regulatory standards, and troubleshooting unexpected deviations in product quality. To address these challenges, it is important to develop strong organizational skills, maintain up-to-date knowledge of industry regulations, and communicate effectively with both production and laboratory teams. Proactively participating in training sessions and collaborating with colleagues can also help ensure consistent quality and foster a supportive work environment.

What is the difference between Quality Control Associate Ii vs Quality Control Associate I?

AspectQuality Control Associate IiQuality Control Associate I
CredentialsTypically requires an associate degree or equivalent; some roles may prefer certifications like CQEHigh school diploma or equivalent; entry-level position
Work EnvironmentLaboratory or manufacturing settings, performing inspections and testsSimilar environments, often with less complex testing responsibilities
ResponsibilitiesPerforming routine quality checks, documenting results, assisting in investigationsAssisting with basic inspections and data collection
Experience LevelUsually 1-3 years of related experienceEntry-level, minimal experience required

In summary, the Quality Control Associate II typically has more experience and may hold certifications, performing more complex testing and analysis compared to the Quality Control Associate I, which is an entry-level role with basic inspection duties.

What does a quality control associate do?

A Quality Control Associate II is responsible for inspecting products, materials, or processes to ensure they meet quality standards and specifications. They perform tests, document findings, and collaborate with production teams to address quality issues, often using tools like measurement instruments and quality management systems. Attention to detail and adherence to safety protocols are essential in this role.

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For Quality Control Associate Ii jobs, the most frequently searched job titles are:

Quality Control Associate Ii jobs near you

Associate II, Quality Control Biology (Temporary)

San Diego, CA • On-site

Artiva Biotherapeutics Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about Artiva Biotherapeutics Inc.external

Other

Posted 25 days ago

Job description

About Artiva:

We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK® is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.

For more information, visit
www.artivabio.com.

Job Summary:

Artiva Biotherapeutics is seeking a skilled and motived QC Associate II, QC Biology (Temporary) who will be reporting to the Associate Director, Quality Control. This individual will perform routine cGMP release and stability testing of Artiva's NK cell therapy products, support laboratory investigations, and contribute to continuous improvement of QC systems. The contract will be through the end of the year with possible extension beyond that.

Duties/Responsibilities:
  • Assist in ordering supplies, reagents and equipment.
  • Write and revise SOPs/Test methods that support Artiva’s cell therapy products.
  • Operate and test ELISA, Flow Cytometers, automated cell counters, and other analytical instruments and equipment, as needed.
  • Support activities for QC equipment IQ/OQ/PQs.
  • Perform routine cGMP release and stability testing of Artiva’s products; including biological tests, biochemistry, chemistry-based tests as needed.
  • Support and as needed evaluate QC systems and/or implement system improvements with supervision.
  • Support laboratory investigations and write reports for deviations and Out of Specification results.
  • Document lab work in a thorough and accurate manner.
  • Perform all work according to company policies, SOPs, and cGMP practices.
  • Assist in planning for GMP release testing, including testing schedules, reviewing biology data and investigating OOS and OOT results.
  • Write technical QC protocols and reports as needed.
  • Assist in analytical qualification and validation, as necessary.
  • Support the transfer and optimization of analytical methods from Analytical Development (or contract laboratories).
  • Develop an in-depth understanding of NK products, testing, and safety.
  • Maintain records and databases in accordance with procedures.
  • Support other special QC projects as needed.
Qualifications:
  • Bachelor’s degree (BS/BA) or relevant scientific field, preferably in biology or related field.
  • Minimum 2 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • Knowledge and experience in supporting cGMP deviations, OOS, etc.
  • Basic knowledge of method transfers, qualifications, and validations; current industry practices; and some experience with guidance interpretation and application
  • Adept at learning critical thinking and technical writing skills.
  • Computer skills required to operate Microsoft Word and Excel programs.

Base Salary: $ 74,000 - $ 85,000. Exact compensation may vary based on level, skills and experience.

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