Job Description

Conducts routine and non-routine analysis of raw materials, in-process items, and finished formulations according to standard operating procedures. Performs biochemical and/or chemical analyses to ensure product stability and compliance with specifications. Compiles data for documentation of test procedures, including biochemical and chemical assays, stability program testing, and formulation studies. Calibrates and maintains laboratory equipment, participates in investigations, and prepares summaries and reports. May develop testing methods, revise SOPs, and perform special projects related to analytical and instrument problem-solving.

Key Responsibilities

• Conduct routine and non-routine analysis of raw materials, in-process items, and finished formulations.
• Perform biochemical and/or chemical analyses to ensure stability and compliance with established procedures.
• Compile data for documentation of test procedures, including assays and stability testing.
• Calibrate and maintain laboratory equipment.
• Participate in investigations and prepare summaries and reports.
• Develop and validate testing methods as needed.
• Review data for compliance with specifications and report abnormalities.
• Revise and update standard operating procedures.
• Perform special projects on analytical and instrument problem-solving.

Qualifications

Bachelor's or Master's Degree in Chemistry, Biology, Biochemistry, or related field

• Generally requires minimal to no prior relevant work experience

Preferred Qualifications

• Experience in a regulated industry (pharmaceutical, biotech, or medical devices).
• Familiarity with GMP, GLP, and ISO standards.
• Knowledge of analytical techniques such as spectroscopy, ELISA, IHC and microbiological testing.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least January 15, 2026 or until the job is no longer posted.

The full-time equivalent pay range for this position is $29.06 - $45.40/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:

No

Shift:

Day

Duration:

No End Date

Job Function:

Quality/Regulatory