Validation Lead with Veeva / Veeva Clinical at Cognizant - Thailand

Cogswell, North Dakota, United States -

Full Time

Start Date

Immediate

Expiry Date

04 Feb, 26

Salary

112500.0

Posted On

06 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Veeva Clinical, Document Management Systems, Quality Assurance, Regulatory Compliance, GxP Regulations, Validation Lifecycle, Risk Assessment, Agile, Waterfall, HP ALM, JIRA, ServiceNow, Data Validation, Integration Testing, CAPA Management, Process Harmonization

Industry

IT Services and IT Consulting

Description

About the role As a Validation Lead with Veeva DMS/QMS /Veeva Clinical, you will make an impact by driving the validation strategy and execution for Document Management Systems within the life sciences domain. You will be a valued member of the Quality Engineering & Assurance team and work collaboratively with cross-functional stakeholders including QA, IT, and business units to ensure compliance and efficiency across validation processes. In this role, you will: · Lead the testing strategy for Document Management Systems, ensuring robust and efficient processes. · Oversee interoperability validation to guarantee seamless integration across platforms. · Coordinate Computer System Validation (CSV) activities to ensure compliance with regulatory standards. · Utilize ALM tools to manage and streamline testing workflows. · Collaborate with research and development teams to align testing with project goals. · Develop comprehensive test plans and cases to cover all functional and non-functional requirements. · Mentor and guide junior testers, fostering a culture of continuous improvement. · Drive innovation in testing methodologies to improve efficiency and effectiveness. · Monitor and report on testing progress, identifying and addressing any issues promptly. · Ensure all testing activities adhere to company policies and industry best practices. Work model: We believe hybrid work is the way forward as we strive to provide flexibility wherever possible. Based on this role’s business requirements, this is a hybrid position requiring 3 days a week in a client or Cognizant office in Boston, MA. Regardless of your working arrangement, we are here to support a healthy work-life balance though our various wellbeing programs. The working arrangements for this role are accurate as of the date of posting. This may change based on the project you’re engaged in, as well as business and client requirements. Rest assured; we will always be clear about role expectations. What you need to have to be considered · Experience with Veeva Clinical or Veeva DMS/QMS platforms. Strong experience in Clinical and Regulatory domains and systems like Veeva Vault QMS, DMS (Preferred) · Deep knowledge of GxP regulations and global compliance standards (FDA, EMA, MHRA, 21 CFR Part 11, Annex 11, GAMP 5). · Expertise in managing the full validation lifecycle: URS, Risk Assessment, IQ/OQ/PQ, Traceability Matrix, and Validation Summary Reports. · Strong documentation and audit readiness skills, including SOPs and compliance documentation. Proven experience in the life sciences domain, especially in Clinical and Regulatory systems, Familiarity with pharmaceutical industry, · Ability to lead cross-functional teams and manage validation deliverables across geographies. · Proficiency in risk-based validation, deviation handling, CAPA management, and process harmonization. · Familiarity with Agile, Waterfall, and V-Model SDLC approaches. · Technical proficiency in tools like HP ALM, JIRA, ServiceNow, SharePoint. Comfortable with data validation, integration testing, and analytics platforms This will help you stand out Strong stakeholder engagement and communication skills. Proactive approach to problem-solving and process improvement. Commitment to continuous learning and professional development. Experience mentoring junior team members and fostering team growth. Cognizant will only consider applicants for this position who are legally authorized to work in the United States without company sponsorship We're excited to meet people who share our mission and can make an impact in a variety of ways. Don't hesitate to apply, even if you only meet the minimum requirements listed. Think about your transferable experiences and unique skills that make you stand out as someone who can bring new and exciting things to this role. Salary and Other Compensation: Applications will be accepted until November 15th, 2025 The annual salary for this position is between $71,100 to 112,500 depending on experience and other qualifications of the successful candidate. This position is also eligible for Cognizant’s discretionary annual incentive program, based on performance and subject to the terms of Cognizant’s applicable plans. Benefits: Cognizant offers the following benefits for this position, subject to applicable eligibility requirements: Medical/Dental/Vision/Life Insurance Paid holidays plus Paid Time Off 401(k) plan and contributions Long-term/Short-term Disability Paid Parental Leave Employee Stock Purchase Plan Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

As a Validation Lead, you will drive the validation strategy and execution for Document Management Systems in the life sciences domain. You will collaborate with cross-functional teams to ensure compliance and efficiency across validation processes.