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Amgen

Makes biotech medicines for serious illnesses

Principal Engineer

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeThousand Oaks, CA, USA

About the Job

Requirements

  • A doctorate degree and 2 years of engineering or operations experience, or a master's degree and 4 years, or a bachelor's degree and 6 years, or an associate's degree and 10 years, or a high school diploma or GED and 12 years.
  • Advanced degree in Engineering, Biotechnology, Pharmaceutics, or a related discipline, with experience in pharmaceutical development and manufacturing.
  • At least 5 years of relevant experience in pharmaceutical or biotechnology development.
  • Experience designing drug product unit operations such as freeze/thaw, formulation/mixing, filtration, filling, lyophilization, capping, and visual inspection.
  • Experience transferring drug product processes to manufacturing sites.
  • Strong skills in applying fundamental engineering and scientific principles to process design.
  • Experience in recipe development using offline pilot capabilities or in a manufacturing environment.
  • Experience leveraging artificial intelligence and generative AI tools to drive automation, enhance data analysis, optimize workflows, and develop AI-powered solutions for business and operational efficiency.
  • Proficiency in digital technologies and automation systems related to aseptic processing and filling operations, including data analytics, process monitoring tools, and digital process control systems.
  • Experience with process technology transfer, process characterization and validation, and statistical software such as JMP or Minitab.
  • Familiarity with FDA and EU Good Manufacturing Practice standards and global regulatory requirements.
  • Strong project management and cross-functional leadership skills.
  • Experience involving new product development, aseptic processing, filling, lyophilization, manual or automated visual inspection, process characterization, equipment design and implementation, technical transfers to global manufacturing sites, statistical process control, and statistical design and analysis of experiments.
  • Ability to learn and act on dynamic information at a rapid pace.
  • Excellent written and verbal communication.

Responsibilities

  • Lead the design and execution of process development for aseptic filling, lyophilization, and visual inspection.
  • Apply comprehensive knowledge of process and product commercialization to develop and standardize tools that improve business-process efficiency and harmonization, including study designs, prior-knowledge assessments, lessons learned, and protocol and report templates.
  • Partner with unit operation owners and subject matter experts to advance process development activities.
  • Partner with cross-functional subject matter experts across the drug product manufacturing network to execute filling, lyophilization, and visual inspection characterization and recipe development, enabling technology transfers and new product introductions across clinical and commercial manufacturing sites.
  • Collaborate across functions to identify and implement process improvements, provide technical support, and facilitate knowledge sharing across sites.
  • Analyze data using advanced statistical and analytical techniques and statistical software.
  • Support clinical and commercial fill/finish manufacturing as needed through process capability analysis, troubleshooting, root-cause analysis, and product impact assessments for nonconformance investigations and process changes or improvements.
  • Apply and advance in silico modeling tools.
  • Author and review guidance documents, technical protocols and reports, product impact assessments, and regulatory sections supporting investigational new drug and marketing application submissions.
  • Provide progress reports and presentations that keep management informed and engaged on program status, advancement, and future functional needs.
  • Periodically support authorship of manuscripts and technical articles, departmental workshops, and evaluations of offline capabilities.

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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