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Biotech Quality Control Jobs in California (NOW HIRING)

The QC Inspector examines items for defects in materials, work, and damage. The Inspector is ... pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is ...

QC Manager - Simply Biotech OVERVIEW Are you looking for a new career opportunity with an exciting biotech company?! Then we have got the right team for you! In this role, you are responsible for the ...

Quality Control Inspector Are you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our ...

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ...

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 ...

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Control Inspector inspects materials, parts, and products at different ...

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Biotech Quality Control information

See California salary details

$30.1K

$80.3K

$127.8K

How much do biotech quality control jobs pay per year?

As of Jul 26, 2026, the average yearly pay for biotech quality control in California is $80,259.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,700.00 and $98,700.00 per year, depending on experience, location, and employer.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
What are the most commonly searched types of Biotech Quality Control jobs in California? The most popular types of Biotech Quality Control jobs in California are:
What are popular job titles related to Biotech Quality Control jobs in California? For Biotech Quality Control jobs in California, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in California look for? The top searched job categories for Biotech Quality Control jobs in California are:
What cities in California are hiring for Biotech Quality Control jobs? Cities in California with the most Biotech Quality Control job openings:
Infographic showing various Biotech Quality Control job openings in California as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 89% Full Time, 5% Part Time, and 4% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $80,259 per year, or $38.6 per hour.
Quality Control Inspector

Quality Control Inspector

KORE1 Technologies

Irvine, CA • On-site

$26 - $28/hr

Contractor

Posted 16 days ago


Job description

KORE1, a nationwide provider of staffing and recruiting solutions, has an immediate opening for a Quality Control Inspector in Irvine, Ca
About the Role:
The Quality Control (QC) Inspector inspects purchased parts, assemblies, accessories, and materials for conformance to requirements and specifications. The QC Inspector examines items for defects in materials, work, and damage. The Inspector is responsible for ensuring conformance of incoming materials to the requirements of medical device components and finished goods.
Essential Duties and Responsibilities:
* Performs visual, dimensional and functional inspection and testing according to documented policies and procedures.
* Records inspection and test data as prescribed by written instructions and procedures.
* Reviews supplier-provided documentation to determine compliance with specifications and drawings; maintains accurate and complete records for each part, including the Receiving Inspection (RI) log; completes, scans, and files RI quality records; and ensures status is updated electronically in the Enterprise Resource Planning system.
* Label all inspected components and materials accordingly, following visual inspection and final disposition.
* Work collaboratively and communicate proactively with Procurement, R&D Engineering, Manufacturing Engineering, Receiving, and other departments to ensure timely and high-quality execution of RI responsibilities.
* Strictly comply with standard operating procedures and work instructions, recommending improvements and enhancements to processes, and performing other duties as determined by management.
Qualifications / Job Requirements:
* High school diploma / GED or an equivalent combination of education and work experience.
* A minimum of 1-3 years' experience working in a regulated environment, medical device or pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is preferred.
* Experience with incoming or in-process inspection, able to read and understand Engineering Drawings and Part Specifications.
* Experience participating in cross-functional teams to support business priorities is preferred.
* Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
* Able to use measuring equipment such as calipers, micrometers, gages, etc.
* Proficient in MS Office programs including Word, Excel and Arena is a plus.
* Strong understanding of quality control standards and testing techniques preferred.
* Result-oriented, positive 'can-do' attitude with demonstration of appropriate urgency and initiative.
Job Requirements
Compensation depends on experience but is typically 26-28/hr.
ABOUT KORE1
Specializing in professional and technical recruiting, KORE1 is committed to supporting top IT, Engineering, Creative, Scientific, Accounting and Finance professionals in their career paths. We build deep relationships with leading companies, connecting them to exceptional talent every day. With extensive industry expertise and unmatched opportunities, our goal is to provide a unique experience for our contractors and consultants as they prepare for their next role. We are passionate about matching the right people with the right companies.
Kore1 provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Kore1 complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Kore1 expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Kore1's employees to perform their job duties may result in discipline up to and including discharge.