Validation Engineer - Clinical Data Hub

Hyderabad, Telangana
Permanent
Full-time

1 month ago

Career Category EngineeringJob DescriptionJoin Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Validation Engineer - Clinical Data HubWhat you will doLet’s do this. Let’s change the world. In this vital role You will play a key role in a content automation initiative which will modernize and digitize the regulatory submission process, positioning Amgen as a leader in regulatory innovation. The initiative demonstrates state-of-the-art technologies, including Generative AI, Structured Content Management, and integrated data to automate the creation, review, and approval of regulatory content.Role Description:We are seeking an Validation Engineer to work on a GxP platform supporting the Regulatory Submission system and Clinical Data Hub platform. This role will be pivotal in ensuring compliance, efficiency, and innovation in the management of data validation processes. The successful candidate will work on a small team and support continuous improvements and automation within the platform. This position combines technical expertise, validation experience, and a strong understanding of GXP requirements.The role also leverages domain and business process expertise to drive ongoing improvements to validation and meets our regulatory and validation procedures. This role involves working closely with developers and business analysts to ensure that the technical requirements for upcoming development are thoroughly elaborated and validated.Roles & Responsibilities:

Develop comprehensive test plans and strategies based on project specifications and requirements.
Perform manual and automated testing of software applications, including functional, regression, and performance testing.
Document and report defects identified during testing and collaborate with development teams for resolution.
Maintain detailed records of test plans, test cases, and test results to ensure traceability and compliance.
Validate test scenarios against feature acceptance criteria and customer expectations.
Ensure system compliance with regulatory requirements for data integrity, traceability, and reliability.
Find opportunities to enhance testing efficiency and minimize manual efforts.
Evaluate and adopt tools and technologies to improve automation capabilities.
Keep validation documentation updated and aligned with GxP standards.
Ensure strict alignment to organizational change processes for validated systems.
Stay informed on industry trends, emerging technologies, and regulatory updates relevant to GxP.
Provide expert technical support in validation to optimize quality, efficiency, and cost for developing, troubleshooting, and improving new and existing applications and platforms.

What we expect of youWe are all different, yet we all use our unique contributions to serve patients.Basic Qualifications and Experience:

Master's degree / Bachelor's degree and 5 to 9 years.

Functional Skills:Must-Have Skills:

Excellent problem-solving skills and a passion for tackling complex challenges in Clinical Development with technology
Experience with Agile software development methodologies
Proficiency in automation tools, data systems, and validation software.
Excellent communication skills and the ability to interface with senior leadership with confidence and clarity
Excellent collaboration, communication, must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment.
Experience in writing requirements for development of modern web application
Strong understanding of GAMP 5 guidelines, 21 CFR Part 11, and Annex 11.
Have strong business acumen. Can demonstrate a deep understanding of pharma industry regulations and its compliance requirements

Good-to-Have Skills:

Demonstrated expertise in a scientific domain area and related technology needs
Understanding of scientific software systems strategy, governance, and infrastructure
Familiarity with low-code, no-code test automation software
Experience in the software development lifecycle of GxP Systems.
Technical thought leadership
Able to communicate technical or complex subject matters in business terms
Knowledge of DevOps, Continuous Integration, and Continuous Delivery methodology
Strong analytical/critical-thinking and decision-making abilities.
Ability to work effectively in a fast-paced, dynamic environment.
Established business partnerships and IS governance practices involving senior business stakeholders
Broad working knowledge of key IS domains and layers

Professional Certifications:

SAFe for Teams certification (preferred)

Soft Skills:

Able to work under minimal supervision
Skilled in providing oversight and mentoring team members. Demonstrated ability in effectively delegating work
Excellent analytical and gap/fit assessment skills
Strong verbal and written communication skills
Ability to work effectively with global, virtual teams
High degree of initiative and self-motivation
Ability to manage multiple priorities successfully
Team-oriented, with a focus on achieving team goals
Strong presentation and public speaking skills

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.

What you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.Apply now and make a lasting impact with the Amgen team.careers.amgen.comAs an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided 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 accommodation..

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