LabWare LIMS Technical Consultant
About the role
As a LabWare LIMS Technical Consultant, you will make an impact by delivering laboratory informatics solutions that support quality, compliance, and operational excellence across pharmaceutical and life sciences organizations. You will be a valued member of the Life Sciences Technology team and work collaboratively with laboratory personnel, quality teams, business stakeholders, and technical teams to implement, enhance, and support LabWare LIMS solutions within regulated environments.
In this role, you will:
- Design, configure, customize, and support LabWare LIMS solutions to meet business, laboratory, and regulatory requirements.
- Lead requirements gathering, solution design workshops, and business process assessments, providing subject matter expertise on LabWare LIMS capabilities and industry best practices.
- Develop and maintain custom LabWare components including LIMS Basic scripts, subroutines, event triggers, visual workflows, calculations, and custom business logic.
- Design and support integrations between LabWare LIMS and enterprise applications, laboratory instruments, SAP, MES, ERP platforms, and third-party systems.
- Collaborate with business and IT teams to optimize laboratory processes, support system enhancements, and ensure successful project delivery across multiple environments.
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 time in a Cognizant or client office as determined by project and business needs. 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
- 8+ years of professional experience, including 5+ years of hands-on LabWare LIMS implementation, configuration, customization, and support experience.
- Strong functional and technical expertise with LabWare LIMS in regulated pharmaceutical, biotechnology, or life sciences environments.
- Deep understanding of LabWare LIMS configuration, workflows, sample lifecycle management, and laboratory business processes.
- Strong experience with LIMS Basic development, including calculations, variable properties, custom algorithms, and business rule implementation.
- Proven expertise in developing subroutines, event triggers, visual workflows, and custom LabWare solutions.
- Experience configuring analyses, sample plans, products, item codes, and laboratory master data.
- Hands-on experience integrating LabWare LIMS with SAP, MES, ERP platforms, laboratory instruments, and external systems.
- Experience working with SOAP and REST web services, parsing scripts, automated data acquisition, and system integration technologies.
- Knowledge of deployment, migration, validation, release management, and software lifecycle processes within regulated environments.
- Excellent communication, consulting, stakeholder management, and problem-solving skills.
These will help you stand out
- Experience leading cross-functional project teams and mentoring functional and technical consultants.
- Knowledge of laboratory informatics, quality control, quality assurance, and manufacturing operations.
- Experience supporting multiple LabWare environments, including Development, QA, UAT, and Production.
- Familiarity with GxP, FDA, MHRA, and related regulatory compliance requirements.
- Experience performing business process optimization and laboratory digital transformation initiatives.
- Strong understanding of validation methodologies, computerized system validation (CSV), and regulatory inspection readiness.
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 August 21,2026.
The annual salary for this position is between $130,000- $150,000 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.
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。
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