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Amgen

Makes biotech medicines for serious illnesses

Manufacturing Specialist 1

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listed

About the Job

Requirements

  • A doctorate, master's, or bachelor's degree and 8–13 years of experience.
  • At least 4 years of experience in biopharmaceutical manufacturing, manufacturing systems, or related technical roles.
  • Demonstrated expertise in at least one manufacturing domain: manufacturing execution systems or electronic batch records (such as Körber PAS-X or similar); finite scheduling or planning systems (such as SAP PP/DS or S/4HANA); manufacturing data systems, sensing, or digital dashboards; or manufacturing performance management and key performance indicator frameworks.
  • Strong understanding of GxP environments, validation concepts, and data integrity principles.
  • Experience translating manufacturing processes into system or digital requirements.
  • Fluency in product management and modern delivery practices, including roadmapping, prioritization, user-centered design, and adoption at scale.
  • Ability to work effectively with technical teams, including data engineers, developers, and user experience/user interface specialists, without being a coder.
  • Experience supporting system implementations, process improvements, or digital initiatives.
  • Ability to manage multiple priorities and contribute to fast-paced, iterative delivery models.

Responsibilities

  • Support deployment of manufacturing capabilities at sites, including manufacturing execution system standardization, documentation automation, and performance management solutions.
  • Participate in knowledge transfer, onboarding, and stabilization activities to support the transition to capability-center-supported capabilities.
  • Work with site subject-matter experts to capture process knowledge, system requirements, and operational constraints.
  • Identify and escalate risks related to process gaps, system readiness, or compliance considerations.
  • Provide subject-matter expertise in manufacturing domains such as manufacturing execution systems and master batch record design and lifecycle; finite scheduling and planning systems; sensing, data integration, and digital control towers; or performance management and key performance indicator frameworks.
  • Translate manufacturing processes into structured system and data requirements.
  • Define guardrails and design principles to guide solution development, including what can be automated, standardized, or scaled.
  • Support evaluation of system impacts, dependencies, and integration requirements.
  • Work with senior managers, product leads, and subject-matter experts to translate business needs into detailed functional requirements.
  • Partner with artificial intelligence/data, user experience/user interface, and engineering teams to align solutions with manufacturing realities and constraints.
  • Contribute to solution design, prototyping, and minimum viable product development.
  • Validate that proposed solutions are fit for purpose, scalable, and aligned with enterprise standards.
  • Assess whether solutions require GxP controls, validation, and documentation.
  • Ensure requirements incorporate data integrity, auditability, and regulatory expectations.
  • Partner with Quality and technical subject-matter experts to ensure compliance by design in solutions.
  • Support preparation of validation inputs and documentation requirements where applicable.
  • Support use cases through the Innovation Velocity Interface lifecycle: intake, evaluation, minimum viable product, pilot, and scale.
  • Contribute to business case inputs, including feasibility, constraints, and expected benefits.
  • Participate in testing, user validation, and deployment activities.
  • Support development of solutions designed for reuse and standardization across multiple sites.
  • Collaborate with site subject-matter experts, manufacturing leaders, and cross-functional partners.
  • Act as a technical translator between manufacturing stakeholders and development teams.
  • Ensure clear communication of requirements, assumptions, and constraints.
  • Support structured engagement that balances delivery speed with quality and compliance.
  • Travel as needed for global stakeholder engagement; travel is limited and periodic.

Desired Qualifications

  • Strong problem-solving and analytical skills, attention to detail, and system-level thinking.
  • Effective communication and collaboration in a cross-functional, global environment.

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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