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Amgen

Makes biotech medicines for serious illnesses

Senior Associate Quality Control

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWest Greenwich, RI, USAIn-person

About the Job

Requirements

  • A master's degree, or a bachelor's degree and 6 months of Quality, Manufacturing, or Operations experience, or an associate's degree and 2 years of Quality, Manufacturing, or Operations experience, or a high school diploma or GED and 4 years of Quality, Manufacturing, or Operations experience.
  • Experience executing analytical or biological testing according to methods or compendia.
  • Experience with quality control analytical systems and/or quality systems.
  • Strong interpersonal, written, and verbal communication skills across all levels of the organization.
  • Ability to work in a team matrix environment and build relationships with partners.
  • Experience leading teams or projects.
  • Ability to identify, manage, and champion innovative projects to advance productivity and enable lean principles across different functions.
  • Experience auditing and defending processes, procedures, and decisions during regulatory inspections.
  • Ability to think innovatively and transform work organizations.
  • Strong technical writing skills in a highly regulated environment.
  • Exposure to operational excellence initiatives.
  • Ability to navigate ambiguity and provide structured problem solving.
  • Demonstrated ability to deliver on schedule.

Responsibilities

  • Ensure facilities, equipment, materials, organization, processes, procedures, and products comply with safety guidelines, current Good Manufacturing Practices, and other applicable regulations.
  • Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks.
  • Operate laboratory equipment and instrumentation.
  • Perform routine raw material testing.
  • Manage the Raw Material Testing Master Schedule.
  • Review and approve assays, documents, and records.
  • Review and approve results in LIMS.
  • Interface with CTL and enter results in LIMS.
  • Serve as the site subject matter expert for specialized testing, including auto-titration, colorimeter, Fourier-transform infrared spectroscopy, and SOR.
  • Support troubleshooting and problem solving.
  • Alert management to quality, compliance, supply, and safety risks.
  • Support technical risk assessments and deviations as a technical subject matter expert.
  • Support and drive continuous improvement initiatives.
  • Provide instruction on several specialty tests.
  • Own documentation for raw material testing procedures.
  • Complete required assigned training to permit execution of required tasks.
  • Perform additional duties as specified by management.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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