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Amgen

Makes biotech medicines for serious illnesses

Engineering Technical Authority Engineer

Technical WritingConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listed

About the Job

Requirements

  • A bachelor's degree in engineering or a related technical discipline; degrees or demonstrated experience in technical communications or information management may also be considered when accompanied by sufficient engineering or technical experience.
  • Five to nine years of work experience.
  • Experience working with engineering standards, specifications, procedures, technical documentation, or controlled document systems in a regulated or highly structured environment.
  • Strong technical writing, editing, document-control, and information-organization skills.
  • Ability to work effectively with subject matter experts and translate technical inputs into clear, usable document content without changing technical intent.
  • Strong organizational skills and ability to manage multiple document revisions, deadlines, reviewers, and approvals simultaneously.
  • Ability to work across global time zones and adjust meeting windows when critical subject-matter expert or stakeholder participation is required.
  • Working knowledge of how external codes, standards, and industry guidance influence engineering requirements; technical ownership remains with the designated Engineering Technical Authority subject-matter expert.
  • Ability to apply engineering fundamentals and technical knowledge to understand requirements, recognize gaps, and engage appropriate subject-matter experts.
  • Ability to quickly develop understanding of unfamiliar technologies, systems, engineering disciplines, codes, and standards and ask questions to clarify requirements.
  • Ability to organize engineering information so requirements and technical knowledge are controlled, searchable, accessible, and usable by the engineering community.
  • Ability to build effective working relationships with Technical Authorities, subject-matter experts, project teams, and global stakeholders, and facilitate technical-content development and review.
  • Ability to understand how engineering standards, project delivery processes, external requirements, and individual technical requirements interact across the engineering lifecycle.
  • Ability to manage multiple documents, stakeholders, reviews, deadlines, and approval workflows while maintaining document quality.

Responsibilities

  • Support Engineering Technical Authorities and subject-matter experts in developing and maintaining engineering standards, specifications, design guidelines, and Engineering Design Library content.
  • Coordinate with engineering disciplines to capture technical requirements and translate subject-matter expert knowledge into clear, actionable engineering documents without changing technical intent.
  • Review existing engineering documents and identify opportunities for improvement, consolidation, clarification, and standardization.
  • Support periodic review and revision of Design Library documents to incorporate lessons learned, technology changes, industry practices, and evolving business needs.
  • Promote consistency in engineering requirements, terminology, document structure, and application across engineering disciplines and sites.
  • Support governance and lifecycle management of engineering standards, specifications, procedures, and related technical content.
  • Support organization, metadata, searchability, and accessibility of Engineering Design Library content.
  • Support development and continuous improvement of Engineering Project Delivery processes, procedures, standard operating procedures, guidance documents, templates, and tools.
  • Work with project delivery and engineering subject-matter experts to document effective practices across the project lifecycle.
  • Support development and revision of engineering requirements associated with project planning, design, execution, commissioning, qualification, and turnover.
  • Capture lessons learned from engineering projects and support incorporation of those lessons into engineering standards and project delivery practices.
  • Identify opportunities to simplify, standardize, and improve engineering processes and project execution.
  • Author and revise engineering standards, specifications, standard operating procedures, procedures, technical guidance, and related engineering documents.
  • Translate complex technical information into clear, concise, and actionable engineering requirements.
  • Facilitate working sessions with subject-matter experts to capture technical knowledge and develop structured engineering content.
  • Coordinate document reviews and work with stakeholders to resolve comments and reach technical alignment.
  • Manage multiple document revisions, reviewers, deadlines, and approval workflows.
  • Support communication of Engineering Standards and Specifications changes to affected stakeholders.
  • Develop process maps, workflows, tables, diagrams, and other tools to improve communication of engineering requirements and processes.
  • Research applicable external codes, standards, and industry guidance to support document development; technical interpretation and ownership of requirements remain with the designated Engineering Technical Authority subject-matter expert.
  • Structure work hours to support U.S., Europe, and Asia stakeholders, preserve focused document-work time, and provide planned overlap for subject-matter expert reviews, global meetings, and Engineering Standards and Specifications change communications.

Desired Qualifications

  • Experience with Microsoft 365, SharePoint, document libraries, metadata and search concepts, and collaboration tools or equivalent engineering knowledge platforms.
  • Foundational knowledge of biotechnology, pharmaceutical manufacturing, life sciences, or another regulated manufacturing environment.
  • Familiarity with engineering drawings, piping and instrumentation diagrams, equipment specifications, design documentation, or capital-project engineering deliverables.
  • Ability to identify opportunities to simplify, standardize, and improve engineering practices, documentation, knowledge management, and project delivery processes.

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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