Job Description- Conducts routine and non-routine analysis of in-process testing according to standard operating procedures. Testing will include UV-Vis, HPLC, LC-MS, Density, IC solution preparation, and basic sample preparation.
- Performs analyses, including biochemical and/or chemical analyses of products, analysis of in-process items and finished products to ensure stability according to established operating procedures.
- Compiles data for documentation of test procedures that may include biochemical and chemical assays.
- Calibrates and maintains lab equipment.
- Participates in the preparation of investigations, summaries, and reports when needed.
- Reviews data obtained for compliance with specifications and reports abnormalities.
- Revises and updates standard operating procedures as needed.
- May perform special projects on analytical and instrument problem-solving.
Work Schedule: 8:00 AM - 4:30 PM. On-site Requirement: This position requires full-time, on-site presence.Qualifications- Bachelor's or Master's Degree.
- Knowledge of FDA requirements.
- Post-graduate, certification, and/or license may be required.
- 2+ years relevant experience.
Additional DetailsThis job has a full time weekly schedule. Applications for this job will be accepted until at least October 28, 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
Travel Required: No
Shift: Day
Duration: No End Date
Job Function: Quality/Regulatory
