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Amgen

Makes biotech medicines for serious illnesses

Validation Lead

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listedIn-person

About the Job

Requirements

  • At least 2 years of validation experience in a good manufacturing practice-regulated environment, such as pharmaceuticals, biotechnology, or medical devices.
  • 5–9 years of overall testing experience, including at least 2 years of validation experience.
  • Experience leading software validation projects.
  • Proficiency in developing and executing validation protocols (Installation Qualification, Operational Qualification, and Performance Qualification), reports, and related documentation.
  • Familiarity with computer system validation and software validation is a plus.
  • Strong problem-solving and analytical skills.
  • Excellent communication and teamwork skills.
  • A bachelor's or master's degree in computer science and engineering is preferred; another engineering field is considered.
  • Experience with automated and computer-controlled systems validation (21 CFR Part 11) is preferred.
  • Strong verbal and written communication skills.
  • Ability to work effectively with global, virtual teams.
  • Ability to manage multiple priorities successfully.
  • Ability to learn quickly, be organized, and be detail-oriented.
  • Strong presentation and public speaking skills.

Responsibilities

  • Plan, coordinate, and lead the execution of validation activities, including qualification and validation of data products and software applications.
  • Develop, review, and approve validation documentation, including Validation Plans, Validation Protocols (Installation Qualification and Operational Qualification), and Validation Reports.
  • Ensure validation strategies meet regulatory requirements and company standards.
  • Write, review, and approve Installation Qualification, Operational Qualification, and Computer System Validation documents.
  • Stay updated on relevant changes to 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.
  • Track validation activity progress and work with the product owner and scrum master to align validation timelines with the overall project plan.
  • Ensure timely completion of validation activities in line with project objectives and schedules.
  • Document validation activities, including deviations, change control, and non-conformance management.
  • Identify opportunities to improve validation processes.
  • Stay current on new technologies, validation trends, and industry best practices to improve validation efficiency.
  • Collaborate and communicate with product teams.

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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