Quality Systems Administrator

Sorry, this job was removed at 06:15 a.m. (CST) on Monday, Aug 11, 2025
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2 Locations
In-Office
112K-175K Annually
Biotech
The Role
Job Description

We are seeking a dedicated professional to ensure and maintain compliance with customer requirements and regulatory standards. This position holds a wide variety of Quality related activities to ensure compliance with applicable regulatory requirements. This includes, but is not limited to, overseeing Quality System programs, participating in audits, documentation reviews, data analysis, developing program metrics and communicating program status to senior leadership.

Job Responsibilities:

  • Oversee the implementation and maintenance of quality systems to ensure compliance with regulatory standards and company procedures.

  • Plan and implement multiple tasks to ensure quality tasks are completed on time and per procedures for projects that require strategic decision-making.

  • Develop actionable metrics and identify remediation plans to ensure site compliance to Quality Systems. Present program-owned data to senior leadership, including appropriate actions to be taken to improve site performance related to responsibility.

  • Lead Quarterly Management review meetings and communicate program requirements and oversight responsibilities to auditors.

  • Provide support for site Regulatory and client audits as requested.

  • Develop and maintain Standard Operating Procedures (SOP's) and conduct ongoing training sessions to maintain program certification requirements.

  • Ensure investigations for Change Controls, Nonconformances, and Out of Specification investigations are performed according to site procedural and Regulatory requirements.

  • Lead TMS activities associated with system ownership and develop TMS Quality System workflows.

  • Lead various projects as necessary, ensuring the precision, accuracy, and reliability of the GMP process and timely delivery.

  • Continuously identify and implement QS program improvements to support compliance and site efficiencies.

  • Solve a broad range of problems of varying scope and complexity, providing strategic solutions to enhance overall quality systems.

Qualifications
  • Bachelor’s or Master’s Degree or equivalent plus directly relevant experience.

  • 8+ years experience in Quality for a biotech / pharmaceutical environment.

  • Demonstrated experience developing remediation plans to ensure site compliance.

  • Experience leading TMS activities.

  • Must have experience with change controls, nonconformance, and Out of Specification investigations.

  • Prior experience preparing and participating in regulatory and client audits.

#LI-DT1

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least June 9, 2025 or until the job is no longer posted.

The full-time equivalent pay range for this position is $111,840.00 - $174,750.00/yr 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 Affirmative Action employer. We value diversity 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 diversity in the workplace 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

Agilent Technologies Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Agilent Technologies and has not been reviewed or approved by Agilent Technologies.

  • Retirement Support The core U.S. package highlights a generous 401(k) match as a strength. Retirement programs are positioned as competitive within the company’s total rewards.
  • Equity Value & Accessibility An Employee Stock Purchase Plan at a discount provides accessible equity and augments total compensation. Ownership opportunities are presented as a notable advantage alongside retirement benefits.
  • Leave & Time Off Breadth Flexible Time Off, company holidays, a personal holiday, and paid volunteer time create a broad leave offering. Time off can accrue into multiple weeks in the first year, supporting flexibility.

Agilent Technologies Insights

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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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