Associate QC: HPLC & CE Analytics

Amgen Foundation, Inc.

Thousand Oaks (CA)

Presencial

USD 90.000 - 130.000

Jornada completa

Hace 6 días
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Competitive benefits
Total Rewards Plan
Flexible work model

Descripción de la vacante

Amgen Inc. is seeking an Associate Quality Control professional to support the QC analytical chemistry team performing HPLC/UHPLC, CE, and related techniques in a GMP environment. You will contribute to testing, data integrity and method documentation.

Under supervision you will document results, maintain equipment, and help implement new methods. A Bachelor’s or equivalent with familiarity in cGMPs and analytical methods is required, with strong attention to detail and communication.

Formación

  • Bachelor’s degree OR Associate’s degree and 6 months of Quality Control, Quality Assurance or related experience OR High school diploma / GED and 2 years of Quality Control, Quality Assurance or related experience
  • Experience with HPLC and/or Capillary Electrophoresis techniques preferred
  • Ability to adhere to regulatory requirements, written procedures and safety guidelines

Responsabilidades

  • Responsible for one or more of the following activities in QC: analytical testing, sample and data management and equipment maintenance.
  • Perform routine laboratory procedures such as sample analysis, standard and solution preparation.
  • Responsible for documenting, compiling, interpreting, reviewing and entering laboratory data.
  • Providing and communicating results, maintaining/operating specialized equipment and drafting and revising documents such as Analytical Methods, SOPs and technical reports.
  • Support introduction of new methods/techniques into the lab.
  • Perform basic assay and instrument troubleshooting.

Conocimientos

Attention to detail
Communication skills
Regulatory compliance understanding

Educación

Bachelor’s degree or Associate’s degree

Herramientas

HPLC
Capillary Electrophoresis (CE)
cGMP knowledge

Descripción del empleo

Amgen Inc. is seeking an Associate Quality Control professional to support the QC analytical chemistry team performing HPLC/UHPLC, CE, and related techniques in a GMP environment. You will contribute to testing, data integrity and method documentation.

Under supervision you will document results, maintain equipment, and help implement new methods. A Bachelor’s or equivalent with familiarity in cGMPs and analytical methods is required, with strong attention to detail and communication.

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