About The Position

At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Requirements

  • High school/GED + 4 years Quality Control OR Associate's + 2 years Quality Control OR Bachelor's + 6 months Quality Control work experience.

Nice To Haves

  • Experience executing analytical/biological testing per Methods and/or Compendia.
  • Experience with QC analytical systems and/or Quality systems.
  • Excellent interpersonal, written and verbal communication skills with all levels within the organization.
  • Ability to work in a team matrix environment and build relationships with partners.
  • Experience leading teams or projects.
  • Identify, manage, and champion innovative projects to advance productivity and enable LEAN principles across different functions.
  • Demonstrated innovative thinking and ability to transform work organizations.
  • Strong technical writing skills within a highly regulated environment.
  • Exposure to Operational Excellence initiatives.
  • Demonstrated ability to navigate through ambiguity and provide structured problem solving.
  • Demonstrated ability to deliver on schedule.

Responsibilities

  • Provide testing support for the QC Night Shift 'Team C' (Saturday - Tuesday from 9:45pm - 8:15am) at Amgen Rhode Island.
  • Ensure that facilities, equipment, materials, organization, processes, procedures and products comply with safety guidelines, cGMP practices and other applicable regulations.
  • Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks.
  • Operate laboratory equipment and instrumentation.
  • Perform review and approval of assays, documents and records.
  • Support troubleshooting and problem solving.
  • Alert management of quality, compliance, supply and safety risks.
  • Support TRAs and deviations, as applicable.
  • Support and drive Continuous Improvement initiatives.
  • Complete required assigned training to permit execution of required tasks.
  • Perform additional duties as specified by management.

Benefits

  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions.
  • Group medical, dental and vision coverage.
  • Life and disability insurance.
  • Flexible spending accounts.
  • A discretionary annual bonus program.
  • Stock-based long-term incentives.
  • Award-winning time-off plans.
  • Flexible work models, including remote and hybrid work arrangements.

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Industry

Chemical Manufacturing

Education Level

High school or GED

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