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Quality Control Associate Two Jobs in California

Astrix Inc

Sr. QC Associate

Fremont, CA · On-site

High School Diploma with 6+ years, Associate Degree with 4+ years, or Bachelor's Degree in a science or engineering field with 2+ years of cGMP experience * Prior Quality Control experience preferred

Pharmaron

Quality Control Associate I / II

Carlsbad, CA · On-site

$25 - $33/hr

Quality Control Associate I / II Location: Carlsbad, CA (on-site) Hourly Range: $25.00 - $33.00 (DOE) About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and ...

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 ...

Sysco Corporation

Quality Control Associate

Union City, CA · On-site

$21.88 - $32.84/hr

Regularly exercises discretion and in performing duties directly related to the general operation of product quality control. RESPONSIBILITIES Provide technical, customer relations, and personnel ...

Sysco

Quality Control Associate

San Francisco, CA

$21.88 - $32.84/hr

Regularly exercises discretion and in performing duties directly related to the general operation of product quality control. RESPONSIBILITIES Provide technical, customer relations, and personnel ...

International Window

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Quality Control Associate

Stockton, CA · On-site

$18.50 - $20/hr

Use Verified by QC · Check insulated glass department log twice daily. Verified by QC · Check finished products and logs twice daily. · Run a 15-minute sill water test and a weep drainage test at ...

Fladger Associates

QC Associate IV

Fremont, CA · On-site

Excellent employment opportunity for a QC Associate IV in the Fremont, CA area. * Reviews raw material lot packages and releases RM lots for GMP manufacturing use. * Ensures lot release timelines ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals. Job Responsibilities: * Perform a broad variety of basic and moderately ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals. Job Responsibilities * Perform a broad variety of basic and moderately complex ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals. Job Responsibilities: * Perform a broad variety of basic and moderately ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals. Job Responsibilities * Perform a broad variety of basic and moderately complex ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals. Job Responsibilities: * Perform a broad variety of basic and moderately ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals. Job Responsibilities: * Perform a broad variety of basic and moderately ...

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All JobsQuality Control Associate Two JobsQuality Control Associate Two Jobs in California

Quality Control Associate Two information

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.

What cities in California are hiring for Quality Control Associate Two jobs? Cities in California with the most Quality Control Associate Two job openings:
Quality Control Associate Two jobs near you
Associate II, Quality Control Biology

Associate II, Quality Control Biology

Artiva Biotherapeutics

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Salary: $79,000 - $91,000 annually. Exact compensation may vary based on level, skills and experience.

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 who will be reporting to the Senior Manager, 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.

Duties/Responsibilities:

  • Assist in ordering supplies, reagents and equipment.
  • Write and revise SOPs/Test methods that support Artivas 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 Artivas 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:

  • Bachelors 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.


In addition to a great culture, we offer:

  • A beautiful facility
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.

If all this speaks to you, come join us on our journey!

Base Salary: $ 79,000 - $ 91,000. Exact compensation may vary based on level, skills and experience.