Agilent Technologies

Document Control II

Agilent Technologies  •  $25.54 - $39.90/hr  •  Frederick, MD (Onsite)  •  16 days ago
Apply
AI can make mistakes so check important info. Chat history is never stored.
40
AI Success™

Job Description

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com

We are currently hiring a Document Control II to join our team in Frederick, CO.

Responsibilities:

  • Handles the document lifecycle using the site Training and Document Management System (TMS)

  • Maintains all document files as related to Agilent NASD and assists in the archival of documents at the offsite storage location

  • Issues and reconciles controlled documentation including logbooks, notebooks, controlled forms, batch records, and protocols

  • Plans and executes multiple tasks to ensure controlled documents are prepared on time, managed per procedures, and align with applicable regulations

  • Provides training to Agilent personnel on TMS and related processes

  • Generates, reviews, and approves labeling materials

  • Represents Document Control (DC) in internal meetings, customer interactions, and Regulatory inspections

  • Provides support on various other projects or tasks delegated by Document Control Supervisor

  • Possesses the ability to evaluate processes, identify efficiencies, and motivate change

Shift: 10:00 AM - 6:30 PM MT

Qualifications

Required:

  • High school Diploma or equivalent

  • Skill in using computer software and hardware applications, including Microsoft products (Word, Access and Excel) and the Internet

Desired:

  • Prior experience and/or training working in a GMP production environment

  • Possesses skills in effective communication, written, and verbal

  • Ability to use, maintain, and train in the TMS system

  • Ability to effectively present information and respond to questions from co-workers, managers, contractors, and customers

  • Responsible for managing various projects

  • Knowledge of GMP guidelines as well as international conference on harmonization (ICH) regulations pertaining to the production of APIs and drug products

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least March 26, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $25.54 - $39.90/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/locationsAgilent 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 job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.

Travel Required:

No

Shift:

Day

Duration:

No End Date

Job Function:

Quality/Regulatory

Agilent Technologies

About Agilent Technologies

Agilent customers are finding new ways to treat cancer, ensure food, water, air, and medicine quality and safety, discover new drug treatments, research infectious diseases, and create alternative energy solutions for a greener planet. From start to finish, we have them covered with our vast product solutions and services portfolio.

Around the world, Agilent’s people bring innovations, technologies, and services to the forefront of science. Our teams design and manufacture a wide array of advanced analytical, research, and diagnostic solutions and tools for use inside and outside laboratories.

Additionally, the unique expertise of Agilent’s CrossLab and technical teams provides valuable insight and support to our customers, helping them fully optimize their laboratories and resources to better focus on what's important: bringing great science to life.

In fiscal 2022, Agilent Technologies generated revenue of (US) $6.85 billion.

Industry
Biotech & Life Sciences
Company Size
10,000+ employees
Headquarters
Santa Clara, CA
Year Founded
1999
Social Media