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Qc Associate Jobs in California (NOW HIRING)

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 ...

CYNET SYSTEMS

QC Associate II

Fremont, CA · On-site

$28 - $33/hr

As part of the QC Phys-Chem Testing team, execute and coordinate routine and non-routine testing of bulk drug substance, final finish products, and raw materials within a multi-product facility.

First Staffing Group

Be Seen First

QUALITY CONTROL

Anaheim, CA · On-site

$20.75/hr

QC - Quality Control / Control de Calidad We are seeking an experienced QC Associate (Quality Control / Control de Calidad) for a food manufacturing facility in Anaheim, CA. Pay: $20.75/hour Shifts ...

Accurate Personnel LLC

Quality Control

Roseville, CA

$20/hr

QUALITY CONTROL ASSOCIATE IN ROSEVILLE, CA Accurate Personnel is hiring immediately for a Quality Control Associate to join our team in Roseville, CA. This position is responsible for inspecting ...

Onterris

Reporting QC Associate - Stack

Santa Ana, CA · On-site

$20 - $25/hr

A Day in the Life As a Reporting QC Specialist, you'll be responsible for accurately calculating and validating stack testing results using spreadsheets and handwritten field records. The ...

Alcon3Pl

Quality Control - Anaheim

Anaheim, CA · On-site

$18 - $25/hr

We are seeking an experience quality control asociate to add to our team in our Anaheim warehouse. This is a TEMP TO HIRE POSITION. Position Sumarry: Quality control (production operator) will be ...

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How much do qc associate jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for qc associate in California is $25.13, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $30.62 per hour, depending on experience, location, and employer.

What is a QC associate?

A QC (Quality Control) Associate is a professional responsible for performing tests and inspections on products, materials, or processes to ensure they meet established quality standards. They work primarily in manufacturing, pharmaceutical, biotechnology, or food industries, helping to identify defects and maintain compliance with regulatory requirements. QC Associates document their findings, report issues, and may assist in implementing corrective actions to improve product quality. Their work is critical in ensuring that only safe and effective products reach customers.

What skills and qualifications are needed to be a QC associate?

To thrive as a QC Associate, you need a background in chemistry, biology, or a related scientific field, often supported by a relevant degree or laboratory experience. Familiarity with laboratory equipment, analytical instruments (like HPLC or GC), and quality management systems (such as GMP or ISO standards) is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring accuracy and collaborating with team members. These competencies are essential for maintaining product quality, regulatory compliance, and operational efficiency in quality control environments.

What challenges do QC associates face when ensuring product quality, and how can they be addressed?

QC Associates often encounter challenges such as tight production deadlines, handling multiple testing protocols, and maintaining accuracy under pressure. Adapting to new technologies or updated regulatory standards can also present difficulties. To address these, strong organizational skills, continuous training, and effective communication with cross-functional teams are essential. Additionally, maintaining thorough documentation and proactively identifying potential issues can help ensure consistent product quality and compliance.

What are the most commonly searched types of Qc jobs in California?

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Qc Associate jobs near you
Infographic showing various Qc Associate job openings in California as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $52,269 per year, or $25.1 per hour.

Quality Control Associate, Microbiology

Carlsbad, CA • On-site

Argonaut Manufacturing Services
Biotechnology Research and Development • 51 - 200 employees
Learn more about Argonaut Manufacturing Servicesexternal

$27 - $32/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago

Job description

Corporate Overview
Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.
Benefits and Pay Range
Benefits for this position, subject to applicable eligibility requirements.
  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Company Paid Life Insurance 1X annual Salary
  • Voluntary Life Insurance
  • Long-Term Disability Insurance and Short-Term Disability Insurance
  • Flexible Spending Account and Health Saving Account
  • 401(K) Retirement Plan
  • 10 Days of Paid Time Off
  • 10 Paid Holidays Annually
The pay range for this position is between $27.00 - $32.00 per hour. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.
Position and Scope
The purpose of this position is to assist in establishing and managing a microbiology program that oversees aseptic fill/finish activities, environmental monitoring, gowning qualification, and the establishment of compendial microbiology assays that include endotoxin, bioburden, and sterility. The position is responsible for ensuring all activities are performed within an appropriate level of cGMP compliance. Previous experience with aseptic filling operations and controls and drug product process validation is highly desired.
This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 6:00am and 9:00am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance.
Responsibilities and Duties
  • Serve as a subject matter expert (SME) for Microbiological assays and methods during internal/external audits, risk assessments, investigations, and client visits
  • Supports assay transfer, qualification, and validation activities for microbial based assays or clients' specific methods
  • Author, revise, and review Quality Control (QC) standard operating procedures (SOPs) and assay qualification protocols and reports
  • Perform analysis on in-process samples, APIs, raw materials, and stability samples using existing methods
  • Perform routine and non-routine environmental monitoring (EM) of GMP and GLP manufacturing facilities for total particulates, air viables, and surface viables.
  • Initiate and participate in the investigation of environmental monitoring excursions and assesses potential impact on product quality
  • Support a Gowning Qualification Program for all manufacturing and QC personnel
  • Perform routine monitoring of pharmaceutical water and gas systems
  • Perform Bioburden, Growth Promotion, Endotoxin, Gram Stain, Microscopy, TOC, Conductivity, and Nitrates testing
  • Maintain QC lab equipment and provide assistance, as needed, during equipment and facility qualification activities
  • Assist in trending EM data and generate quarterly and yearly reports
  • Participate in inspection readiness activities
  • Interact closely with other departments to ensure efficient, compliant, and timely execution of project activities
  • Provide assistance as needed to maintain a functioning QC Laboratory, including material ordering, inventory control, general housekeeping, and other duties
  • Assist in investigation and review of GMP quality events, including but not limited to deviations, non-conformances, and audit findings
  • Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results with a client driven focus
  • Safely operate laboratory equipment in accordance to established practices and SOPs
  • Assist in training of additional team members
  • Under minimum supervision, support special projects as needed
  • Operates to the highest ethical and moral standards.
  • Adheres to quality standards set by regulations and Argonaut Manufacturing Services policies and procedures
  • Communicates effectively with supervisors, staff, and clients
  • Participate in projects within a team and as an individual
  • Support continuous improvement projects related to QC
  • Multi-task, prioritize workload, document properly and interpret data accurately
  • Follow laboratory safety requirements to promote a safety-first culture
Requirements and Qualifications
  • Combination of Undergraduate courses and on-the-job experience in Microbiology or a related discipline (e.g., biology, chemistry, or biological sciences)
  • Minimum three (3) years' experience in Quality Control and environmental monitoring of GMP facilities
  • High intelligence and problem-solving skills
  • Excellent oral and written communication and listening skills
  • High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction
  • Experience in a growth-oriented, cGMP contract manufacturing organization with a focus on compliant execution of business is preferred
  • General knowledge of one or more of compendial methods such as: Bioburden, Endotoxin, Growth Promotion, Sterility, and other microbiological methods
  • Knowledge in environmental excursion investigations, root cause analysis, out of specifications, and knowledge of cleanroom practices is preferred
  • Direct experience with endotoxin, bioburden, and growth promotion methodologies. Experience in sterility testing is highly desired.
  • Experience with transfers and qualification/validations of large molecule focused analytical methods
  • Must have experience with Microsoft Office applications
  • Experience with quality software and 21 CFR 11 applications preferred

Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies with all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.

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