Sr Associate IS Test Engineer

Amgen Inc. (IR); Hyderabad; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

Amgen Inc. is seeking a Sr Associate IS Test Engineer to join a collaborative team ensuring quality for enterprise applications in a GxP environment. You will design manual and automated tests, support UAT with stakeholders, and maintain validation documents through the test lifecycle.

Responsibilities include OQ/regression testing, defect tracking in JIRA/HP ALM, and building automation scripts with Selenium/TestNG to ensure compliant, audit-ready delivery across platforms.

Qualifications

• Master’s/Bachelor’s degree in Computer Science, IT or related field.
• Experience in designing and executing manual and automated tests.
• Strong knowledge of validation standards and GxP/CSV requirements.

Responsibilities

• Design and develop manual and automated test cases based on requirements.
• Maintain RTM for full test coverage and support UAT.
• Log and track defects ensuring traceability and re-testing after fixes.
• Execute OQ and regression tests and document results.
• Support automation by building and maintaining scripts in Selenium/TestNG.

Skills

Manual testing

Automated testing

Test design

UAT support

Defect tracking

Education

Master’s/Bachelor’s degree in Computer Science/IT

Tools

Selenium

TestNG

Postman

JIRA

HP ALM

qTest

Jenkins

GitHub Actions

Job description

Career Category Engineering Job Description

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

About the Role

Role Description: As a Sr Associate IS Test Engineer, you will join a collaborative team implementing and supporting the next generation of safety platforms and supporting technologies. In this role, you will be responsible for ensuring the quality and compliance of enterprise applications, with a strong focus on test planning, execution, defect management, and test automation. You will work closely with product owners, developers, and QA teams to validate systems against business and regulatory requirements. Your expertise in automation testing, along with manual testing knowledge, will contribute to delivering robust solutions across platforms such as Medical Information Websites and other validated systems. This role is critical in ensuring that applications meet performance, security, and compliance expectations across the development lifecycle, especially in GxP-regulated environments.

Roles & Responsibilities

• Design and develop manual and automated test cases based on functional and non-functional requirements.
• Create and maintain the Requirement Traceability Matrix (RTM) to ensure full test coverage.
• Assist in User Acceptance Testing (UAT), working closely with business stakeholders.
• Set up test data based on preconditions identified in test cases.
• Execute tests including Dry Runs, Operational Qualification (OQ), and regression testing.
• Capture test evidence and document test results in accordance with validation standards.
• Log and track defects using tools such as JIRA or HP ALM, ensuring clear documentation and traceability.
• Ensure defects are re‑tested post‑fix and verified for closure in collaboration with development teams.
• Execute test scripts provided by analysts, focusing on accuracy and completeness of testing.
• Collaborate with developers to ensure all identified bugs and issues are addressed and resolved effectively.
• Support automation testing efforts by building and maintaining scripts in tools like Selenium, TestNG, or similar.
• Maintain detailed documentation of test cycles, supporting audit readiness and compliance.
• Ability to perform responsibilities in compliance with GxP and Computer System Validation (CSV) regulations, ensuring proper documentation, execution, and adherence to regulatory standards.

Basic Qualifications and Experience

Master’s/ Bachelor’s degree and 5 to 9 years of Computer Science, IT or related field experience

Functional Skills

Must-Have Skills: Strong experience in designing and executing both manual and automated test cases based on functional and non-functional requirements. Hands‑on expertise in building and maintaining automated functional, regression, and integration tests scripts using tools such as Selenium, TestNG, Postman, or similar, enabling scalable and reusable test automation. Proficient in using tools like JIRA, HP ALM, or qTest for defect logging, tracking, test execution, and traceability, ensuring audit readiness and compliance with validation standards. Familiarity with Jenkins, GitHub Actions, or similar tools for integrating testing into DevOps pipelines. Develop, enhance, and maintain test automation scripts using data‑driven, keyword‑driven, or hybrid frameworks, enabling reusable, scalable, and maintainable test coverage across Salesforce and integrated systems. Proficient in creating test lifecycle documentation (RTMs, OQ protocols, test plans, reports) and supporting end‑to‑end testing within regulated GxP and CSV‑compliant computer systems, ensuring adherence to validation, audit, and documentation standards.

Good-to-Have Skills: Familiarity with performance testing (e.g., JMeter) and API testing using tools like Postman to validate service‑level functionality and performance. Experience working within Agile or Scrum frameworks and supporting continuous testing practices across sprint cycles and iterative releases. Proven ability to work effectively with cross‑functional teams including developers, QA, and business stakeholders to support UAT, validate fixes, and ensure issue resolution throughout the development lifecycle. Background in testing applications in the healthcare or pharmaceutical industry, with an understanding of compliance, patient safety, and regulatory constraints. Ability to manage test data setup and maintain thorough documentation of test evidence to support compliance, audit preparation, and traceability. Experience collaborating with cross‑functional teams, particularly within healthcare or pharmaceutical environments.

Professional Certifications

• ISTQB Foundation or Advanced Level Certification
• Certified Automation Tester (e.g., Selenium WebDriver Certification)
• SAFe Agile or Scrum Certification (optional)
• Certified CSV/Validation Professional (optional)

Soft Skills

Strong attention to detail and documentation quality Excellent analytical and problem‑solving skills Good verbal and written communication skills Ability to work both independently and within a team High accountability and ownership of assigned tasks Adaptability to fast‑paced and evolving environments Strong collaboration skills across functional and technical teams

Shift Information

This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required based on business requirements.

EQUAL OPPORTUNITY STATEMENT

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

For more information, visit www.amgen.com and follow us on www.twitter.com/amgen