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Amgen

Makes biotech medicines for serious illnesses

Validation Associate - Artist

Manual & Functional QAConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's or master's degree and 2 to 4 years of experience in Supply Chain Technology, Supply Chain Business, Engineering, IT, or a related field.
  • Experience in software validation projects.
  • Proficiency in executing validation protocols (IQ, OQ, PQ), reports, and related documentation.
  • Familiarity with computer system validation and software validation is a plus.
  • Experience with automated and computer-controlled systems validation (21 CFR Part 11) is preferred.
  • Strong problem-solving, analytical, and troubleshooting skills.
  • Ability to work effectively with global, virtual teams.
  • Ability to learn quickly, stay organized, and be detail oriented.
  • High degree of initiative and self-motivation.

Responsibilities

  • Execute validation activities, including qualification and validation of data products and software applications.
  • Stay updated on relevant changes to Amgen’s standard operating procedures and ensure validation practices align with evolving standards.
  • Collaborate with quality assurance, system owners, business owners, RunOps, engineering, and platform teams to drive validation activities and meet project deadlines.
  • Ensure timely completion of validation activities in line with project objectives and schedules.
  • Document validation activities, including deviations, change control, and non-conformance management.
  • Stay current on new technologies, validation trends, and industry best practices to improve validation efficiencies.
  • Collaborate and communicate with product teams.
  • Implement the ESKO artwork management system into the existing Amgen ecosystem with applications including VEEVA, SAP, and EDF, and integrations through Workato and Databricks, leveraging Tableau for analytics and reporting.
  • Support validation activities across business and DTI teams, understand technical solutions' impact on business outcomes, and improve return on investment of investments.
  • Lead the overall operation of development, maintenance, and support of required Information Systems services and develop domain knowledge in the assigned area.

Desired Qualifications

  • Experience with automated and computer-controlled systems validation (21 CFR Part 11).

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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