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Agilent Technologies

Provides eProcurement automation and hosted catalogs

LC/MS Applications Scientist - Biocolumns

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWilmington, DE, USA

About the Job

Requirements

  • A Ph.D. degree or equivalent in chemistry, analytical chemistry, biochemistry, or a related field is required.
  • At least four years of experience with biopharmaceutical Critical Quality Attribute (CQA) or purification analysis is required.
  • Experience with High-Performance Liquid Chromatography (HPLC), liquid chromatography/mass spectrometry (LC/MS) instrumentation, software, and sample preparation is required.
  • The candidate must be able to work independently and be self-motivated while contributing collaboratively to multidisciplinary teams.
  • Experience and comfort with technical writing and presentations in English are required.
  • The candidate must be willing to travel to present at conferences and customer sites.

Responsibilities

  • Develop applications for new products supporting the biopharmaceutical market at the Little Falls facility, with an onsite presence four days per week.
  • Contribute to the development of HPLC workflows to improve HPLC and LC/MS biopharmaceutical sample preparation, method development, and data analysis for peptide, oligonucleotide, and protein (monoclonal antibody) therapeutics.
  • Generate product proof points, competitive comparison data, and workflow methods for publication as Application Notes.
  • Design and execute experiments to create reproducible and robust workflows, application notes, whitepapers, and posters that support customer adoption in therapeutic development and quality assurance/quality control manufacturing release.
  • Serve as a technical expert by providing customer presentations, troubleshooting assistance, and field support.
  • Collaborate with Biopharma product marketing and product managers to develop new products and workflow methodologies, bring them to market, and publish application notes.
  • Work with Research and Development on the development and testing of new products and technologies.
  • Support Manufacturing with testing process improvements and consultation on technical issues.
  • Work with the Commercial team to support customer technical questions.

Desired Qualifications

  • Prior biopharmaceutical industry experience is a plus.
  • Prior experience with GLP-1 therapeutics, peptides, diabetes applications, injectables, or drug-product development is a plus.
  • Experience with characterization or testing of Critical Quality Attributes is highly desired.

About the Company

Agilent Technologies

Provides eProcurement automation and hosted catalogs

Agilent Technologies provides eProcurement services that help businesses buy supplies more efficiently. It offers a suite of electronic procurement tools that let clients load their pricing into existing purchasing platforms, access a hosted catalog, and complete transactions digitally without paper. The service connects pricing data to clients’ procurement systems, delivers an online catalog, and supports automated, paperless purchasing workflows. This makes purchasing faster and reduces manual steps. Compared with competitors, Agilent emphasizes automation, quick connectivity between pricing, catalogs, and purchasing platforms, and a reliable, scalable experience backed by its broad product range. The company aims to improve client productivity and lower procurement costs, helping customers buy what they need more easily while keeping prices clear and consistent.

Company size
10,001+
Company stage
IPO
Headquarters
Santa Clara, CA
Founded
1999

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