About this opportunity
Career Category
Information Systems
Job Description
Validation Lead
Role Name: Validation Lead
Department Name: Enterprise Engineering and Analytics (EEA)
Role GCF: 4
Job Family: Software Development Engineer-Test I I
Hiring Manager Name: Asha Rani
ABOUT AMGEN
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:
We seek a skilled Validation Lead to oversee and manage validation activities for data platforms and solutions . As a key contributor, you will collaborate closely with cross-functional teams to ensure that the data and analytics products follow the required validation processes, documentation, and comply with Amgen’s standard operating procedures, policies, and guidelines . Your expertise will be instrumental in ensuring quality and adherence to required standards so that the engineering teams can build and deploy products that are compliant .
Roles & 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 such as Validation Plans, Validation Protocols (IQ/OQ), and Validation Reports.
Ensure validation strategies meet regulatory requirements and company standards.
Write, review, and approve Installation Qualification (IQ), Operational Qualification (OQ), and Computer System Validation documents.
Stay updated on relevant changes to Amgen’s SOPs and ensure validation practices are aligned with evolving standards.
Collaborate with cross-functional teams, including quality assurance, system owners, business owners, RunOps , engineering, and platform teams to drive validation activities and meet project deadlines.
T rack the progress of validation activities and work closely with the product owner and scrum master to ensure validation activities timelines are aligned with the overall project plan.
Ensure timely and effective completion of all validation activities in line with project objectives and schedules.
Ensure proper documentation of validation activities, including deviations, change control, and non-conformance management .
Identify opportunities for process improvements in validation activities.
Stay current on new technologies, validation trends, and industry best practices to improve validation efficiencies.
Collaborate and communicate effectively with the product teams.
Functional Skills:
Must-Have Skills:
2+ year s of experience in validation in a GMP-regulated environment (pharmaceutical, biotech, medical devices, etc.).
5+ to 9 Years overall experience in Testing with 2+ years of experience in validation experience is mandatory.
Experience leading software validation projects.
Proficiency in developing and executing validation protocols (IQ, OQ, PQ), 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.
Good-to-Have Skills:
Experience with automated and computer-controlled systems validation (21 CFR Part 11)
Education and Professional Certifications
Bachelor’s /Masters degree in computer science and engineering preferred, other Engineering field is considered
Soft Skills:
Excellent analytical and troubleshooting 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 .
Ability to learn quickly, be organized and detail oriented.
Strong presentation and public speaking skills.
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.
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Job details
How this role compares
Computed from every other active Information Technology role in our database, not just this employer's listings.
We currently track 1376 comparable Information Technology roles across 76 biopharma companies.
Salary context
183 of 1376 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1376 comparable roles
+ 29 more countries
Seniority mix
693 of 1376 peers have a known seniority level
Therapeutic area mix
1 of 1376 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.