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Quality Control Associate Two Jobs in Carlsbad, CA

BioLegend

Quality Control Associate

San Diego, CA

Job Summary BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow ...

Collabera

QC Associate I

San Diego, CA · On-site

Qualifications Education: BS/MS in Biology/Molecular Biology, biochemistry, chemistry or related discipline 2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based ...

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Quality Control Associate Two information

See Carlsbad, CA salary details

$11

$26

$39

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

As of Sep 4, 2026, the average hourly pay for quality control associate two in Carlsbad, CA is $26.41, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $32.16 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Associate Two vs Quality Control Associate One?

AspectQuality Control Associate TwoQuality Control Associate One
Required CredentialsHigh school diploma or equivalent; some roles may require certifications in GMP or ISO standardsHigh school diploma or equivalent; basic understanding of quality standards
Work EnvironmentManufacturing or laboratory settings, often in regulated industriesSimilar environments, typically in labs or production areas
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing companiesCommonly used in similar industries, often as entry-level roles
Common Search & Comparison IntentYes, often compared to associate level roles to understand responsibilities and requirementsNo, usually the starting point for quality roles

Quality Control Associate Two typically requires more experience or certifications than Quality Control Associate One. It involves more responsibilities in quality inspections and compliance, making it suitable for those with some industry experience. Both roles are common in manufacturing and laboratory environments within regulated industries.

Is quality control a good career path?

Quality Control Associate Two is a role focused on inspecting products, ensuring standards are met, and documenting quality issues. It offers opportunities for skill development in inspection techniques, attention to detail, and familiarity with quality management systems, making it a stable career choice in manufacturing and production industries.

What does a quality control associate do?

A Quality Control Associate is responsible for inspecting products and materials to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or laboratory environments. Attention to detail and knowledge of quality procedures are essential for this role.

What cities near Carlsbad, CA are hiring for Quality Control Associate Two jobs?

Cities near Carlsbad, CA with the most Quality Control Associate Two job openings:

Quality Control Associate Two jobs near you

Associate II, Quality Control Biology (Temporary)

Artiva Biotherapeutics

San Diego, CA • On-site

$74K - $85K/yr

Temporary

Posted 17 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.