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*
コグニザントについて
コグニザント（NASDAQ: CTSH）は、AI Builderおよびテクノロジーサービスプロバイダーとして、お客様にフルスタックのAIソリューションを構築することで、AI投資と企業価値を結ぶ架け橋となっています。業界、ビジネスプロセス、エンジニアリングに関する当社の深い専門知識を活かし、組織固有のビジネス環境をテクノロジー・システムに組み込みます。これにより、人間の可能性を最大限に引き出し、確かな成果を実現するとともに、急速に変化する世界においてグローバル企業が常に一歩先を行くための支援を行っています。 詳細については、cognizant.ai をご覧ください。
雇用に関する追加情報
本募集に記載されている報酬情報は、掲載日時点で正確なものです。Cognizantは、適用される法令に従い、いつでも本情報を変更する権利を留保します。
応募者は、対面またはビデオ会議による面接への参加を求められる場合があります。また、各面接の際に、現在有効な州政府または政府発行の身分証明書の提示を求められる場合があります。
Cognizantは機会均等雇用主です。応募および選考において、人種、肌の色、性別、宗教、信条、性的指向、性自認、国籍、障がい、遺伝情報、妊娠、退役軍人の地位、その他連邦法・州法・地方自治体の法律により保護されるいかなる特性に基づく差別も行いません。
