Description

Job Description

The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.

Performs sampling of raw materials (occasionally with the use of a respirator).
Conducts routine and non-routine analysis of raw materials to support the manufacturing campaigns. When time allows, this analyst will also support in-process testing to support the Frederick team.
Performs analyses, including, but not limited to, biochemical and/or chemical analyses of raw materials, in lab bench testing of raw materials, appearance, FTIR, Identity testing, UV, Karl-Fisher titrations, Acid-Base titrations, HPLC, LC-MS, GC, GC-MS, NMR, ICP-M
Calibrates and maintains lab equipment. Makes mobile phases and other solutions to support raw material testing and other in process testing. Prepares samples and standards to complete lab analyses.
Maintains raw material sample/retain storage and disposal schedule.
Participates in investigations when needed.
Completes on the job training including training on SOP's and 3-Step in lab training on all QC JOB's.
Reviews data related to all lab testing.
Revises and updates standard operating procedures as needed.
May perform special projects on analytical and instrument problem-solving as time allows.

Shift: Day Shift, Monday-Friday

Qualifications

2+ years of relevant experience for this level
Bachelor's degree (B.S.) Analytical Chemistry or related life sciences field.
Knowledge of cGMP guidelines as well as international regulations (i.e., International Committee on Harmonization (ICH) Q7) pertaining to Quality Control programs that support production of APIs, stability and drug product release
Knowledge of FDA regulations and guidelines
Skills in coordinating and handling day to day tasks and working in collaboration to accomplish deadlines and objectives
Knowledge of and skilled in using computer software and hardware applications, including Microsoft Word and Excel
Demonstrated knowledge of analytical equipment and instrumentation, HPLC experience working in a GMP environment is preferred

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least October 29, 2026 or until the job is no longer posted.

The full-time equivalent pay range for this position is $34.00 - $53.13/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 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:

Shift:

Day

Duration:

No End Date

Job Function:

Quality/Regulatory

QC Analyst - Raw Materials

Description

Job Description

Performs sampling of raw materials (occasionally with the use of a respirator).

Conducts routine and non-routine analysis of raw materials to support the manufacturing campaigns. When time allows, this analyst will also support in-process testing to support the Frederick team.

Performs analyses, including, but not limited to, biochemical and/or chemical analyses of raw materials, in lab bench testing of raw materials, appearance, FTIR, Identity testing, UV, Karl-Fisher titrations, Acid-Base titrations, HPLC, LC-MS, GC, GC-MS, NMR, ICP-M

Calibrates and maintains lab equipment. Makes mobile phases and other solutions to support raw material testing and other in process testing. Prepares samples and standards to complete lab analyses.

Maintains raw material sample/retain storage and disposal schedule.

Participates in investigations when needed.

Completes on the job training including training on SOP's and 3-Step in lab training on all QC JOB's.

Reviews data related to all lab testing.

Revises and updates standard operating procedures as needed.

May perform special projects on analytical and instrument problem-solving as time allows.

Shift: Day Shift, Monday-Friday

Qualifications

2+ years of relevant experience for this level

Bachelor's degree (B.S.) Analytical Chemistry or related life sciences field.

Knowledge of cGMP guidelines as well as international regulations (i.e., International Committee on Harmonization (ICH) Q7) pertaining to Quality Control programs that support production of APIs, stability and drug product release

Knowledge of FDA regulations and guidelines

Skills in coordinating and handling day to day tasks and working in collaboration to accomplish deadlines and objectives

Knowledge of and skilled in using computer software and hardware applications, including Microsoft Word and Excel

Demonstrated knowledge of analytical equipment and instrumentation, HPLC experience working in a GMP environment is preferred

Travel Required:

Shift:

Duration:

Job Function:

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