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Amgen

Makes biotech medicines for serious illnesses

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, technical communications, information management, or a related discipline, or equivalent 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; the role coordinates and researches while technical ownership remains with the designated subject matter expert.
  • Five to nine years of work experience.

Responsibilities

  • Maintain assigned Engineering Specifications, Standards and Guidelines and coordinate periodic reviews to improve clarity, consistency, usability, and alignment with applicable industry standards and engineering practices.
  • Provide hands-on support to technical subject matter experts during document updates and revisions, including document-control coordination, incorporating comments, formatting, reference checking, revision history, review-cycle tracking, and preparation for approval.
  • Support development of new Specifications, Standards and Guidelines by coordinating inputs, facilitating working sessions, organizing source material, and progressing drafts through review and approval.
  • Cascade information about new and updated documents to technical authorities and the broader engineering community through the EDL platform and agreed communication channels; maintain change summaries, effective dates, links, and communication records.
  • Maintain an ESS tracker and review calendar; monitor document status, owners, planned revisions, approvals, and publication; identify overdue or high-priority actions; and provide routine status reporting to technical authority leadership.
  • Maintain the operational interface for ESS updates in the EDL environment, including the Updated ESS Documents SharePoint list and related communication process.
  • Post or coordinate publication of approved ESS changes in accordance with technical authority governance.
  • Prepare concise, user-focused update messages covering document title, revision, change summary, effective date, impacted audience, and link to the current version.
  • Maintain a communication record so the technical authority team can confirm updates were cascaded to the intended engineering audience.
  • Work with technical authorities and subject matter experts, engineering discipline leads, Facilities/Utilities, project engineering teams, Quality/Validation stakeholders as applicable, document owners, and digital or knowledge-management platform support.
  • Structure working hours to provide reliable support to U.S., Europe, and Asia stakeholders, preserving focused document-work time and planned overlap for reviews, global meetings, and communications.
  • Observe role boundaries: support the technical authority team without replacing the technical authority of the designated subject matter expert or document owner; technical decisions, interpretations, approvals, and final release authority remain with assigned technical and governance owners.

Desired Qualifications

  • Experience with Microsoft 365, SharePoint, document libraries, metadata/search concepts, and collaboration tools or equivalent engineering knowledge platforms.

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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