About the role
As a Validation Test Lead – Lab Instrumentation / Medical Devices, you will make an impact by ensuring regulatory compliance and validation of software used in medical laboratory instrumentation. You will be a valued member of the quality and compliance team and work collaboratively with cross-functional stakeholders, including regulatory affairs, engineering, and client teams.
In this role, you will:
• Lead the development and execution of validation and testing strategies for regulated software systems
• Document and validate instrument software in accordance with EMA guidelines and GxP requirements
• Perform risk assessments and proactively communicate risks to stakeholders
• Develop validation test cases, software specifications, and supporting documentation (including infrastructure and data flow diagrams)
• Collaborate with cross-functional teams to ensure seamless integration of compliance requirements
Work model
We strive to provide flexibility wherever possible. Based on this role’s business requirements, this is a remote position open to qualified applicants within the United States. Regardless of your working arrangement, we are here to support a healthy work-life balance through 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
• Proven lead-level experience in lab instrumentation or medical device software validation within a regulated (GxP) environment
• Strong knowledge of EMA guidelines, validation lifecycle, and compliance standards
• Expertise in technical documentation, validation test case creation, and specification writing
• Experience conducting risk assessments and validation lifecycle documentation
• Strong communication and stakeholder management skills across cross-functional teams
These will help you stand out
• Experience in pharmaceutical or medical device industry environments
• Familiarity with IT SOPs and regulatory audit readiness
• Proven ability to lead teams and mentor members in validation best practices
• Experience driving process improvements in testing frameworks and tools
• Exposure to automation or innovative testing approaches in regulated environments
Salary and Other Compensation:
Applications will be accepted until June 22, 2026.
The annual salary for this position is between $83,250– $131,500 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
Cognizant will only consider applicants for this position who are legally authorized to work in the United States without company sponsorship.
*Please note, this role is not able to offer visa transfer or sponsorship now or in the future*
关于高知特 (Cognizant)
高知特(Cognizant)（纳斯达克代码：CTSH）作为一家AI Builder和相关技术服务提供商，致力于通过打造全栈AI解决方案，帮助企业将人工智能投资转化为实际价值。公司凭借深厚的行业经验、流程优化和工程技术专长，将企业独特的业务场景融入科技系统，赋能组织释放人才潜能，推动切实成果，并帮助全球企业在瞬息万变的环境中保持领先。如需了解更多详情，敬请访问 cognizant.ai 或关注@cognizant。
补充雇佣信息
薪酬信息截至本职位发布之日为准。Cognizant 保留在适用法律允许的范围内随时修改该信息的权利。
申请人可能需要通过现场面试或视频会议的方式参加面试。此外，候选人在每次面试时可能需要出示其当前所在州或政府签发的有效身份证件。
Cognizant 是一家提供平等就业机会的雇主。在招聘过程中，您的申请和候选资格不会因种族、肤色、性别、宗教、信仰、性取向、性别认同、国籍、残疾、遗传信息、怀孕、退伍军人身份或任何其他受联邦、州或地方法律保护的特征而受到影响。
