Agilent Technologies is a leading company in the field of scientific research and development, and they are seeking a QC Analyst, Associate to conduct routine and non-routine analysis of materials and formulations. The role involves performing biochemical and chemical analyses to ensure product stability and compliance, as well as compiling data and maintaining laboratory equipment.
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
Skills
- Bachelor's or Master's Degree in Chemistry, Biology, Biochemistry, or related field
- Generally requires minimal to no prior relevant work experience
- 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
Benefits
Company Overview
Agilent Technologies addresses the scientific and laboratory management needs of analytical scientists and clinical researchers. It was founded in 1999, and is headquartered in Santa Clara, California, USA, with a workforce of 10001+ employees. Its website is http://www.agilent.com.Company H1B Sponsorship
Agilent Technologies has a track record of offering H1B sponsorships, with 51 in 2025, 56 in 2024, 58 in 2023, 70 in 2022, 64 in 2021, 53 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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