QC Analyst

Posted 17 Days Ago
Be an Early Applicant
Carpinteria, CA
In-Office
34-53
Junior
Biotech
The Role
The QC Analyst performs quality control testing for IHC products, manages lab equipment, documents results, and collaborates with teams to support product lifecycle and improvements.
Summary Generated by Built In
Job Description

Agilent’s Bioreagents business is an industry leader for cancer diagnostics products that help provide trusted answers to customers. We are seeking an energetic and motivated Quality Control Analyst with at least 1 year of experience to join our team. This role focuses on quality control testing to support the full product lifecycle of Immunohistochemistry (IHC) products.

Perform analytical testing to support product release across the entire lifecycle, including:

  • Incoming material inspection and titrations

  • In-process and final QC testing

  • Real-time stability studies

  • Support EQA studies

  • Operate and maintain laboratory equipment and accurately document test results in compliance with quality standards

  • Communicate effectively with the Quality Control management team and manufacturing partners.

  • Participate in continuous improvement initiatives to reduce costs and improve site performance.

  • Troubleshoot and resolve problems of varying scope and complexity.

Qualifications
  • Bachelor’s or Master’s degree in a relevant scientific discipline (or equivalent combination of education and experience).

  • 1+ years of experience in a Quality Control or related laboratory role.

  • Proficiency with office productivity tools (Word, Excel, PowerPoint, databases).

  • Strong teamwork, problem-solving, and organizational skills.

  • Effective verbal and written communication, including technical writing.

  • Ability to manage multiple priorities in a fast-paced environment.

  • Computer skills including the use of Microsoft office suite and understanding of ERP system mechanics.

Preferred Skills

  • Experience in GLP/ISO-compliant environments.

  • Familiarity with GMP, GDP, and standard operating procedures.

  • Knowledge of ISO 13485:2016 Quality Management System requirements.

  • Hands-on experience with histology, microanatomy, and Immunohistochemistry techniques.

  • Some experience operating laboratory instrumentation is preferred.

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least October 15, 2025 or until the job is no longer posted.

The full-time equivalent pay range for this position is $34.16 - $53.37/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email [email protected] or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: 10% of the TimeShift: DayDuration: No End DateJob Function: Quality/Regulatory

Top Skills

Erp Systems
Microsoft Office Suite
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The Company
HQ: Santa Clara, CA
17,369 Employees
Year Founded: 1999

What We Do

Analytical scientists and clinical researchers worldwide rely on Agilent to help fulfill their most complex laboratory demands. Our instruments, software, services and consumables address the full range of scientific and laboratory management needs—so our customers can do what they do best: improve the world around us.

Whether a laboratory is engaged in environmental testing, academic research, medical diagnostics, pharmaceuticals, petrochemicals or food testing, Agilent provides laboratory solutions to meet their full spectrum of needs. We work closely with customers to help address global trends that impact human health and the environment, and to anticipate future scientific needs. Our solutions improve the efficiency of the entire laboratory, from sample prep to data interpretation and management.

Customers trust Agilent for solutions that enable insights...for a better world.

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