Job Responsibilities
Requirements & Analysis
· Engage Business SMEs and Key Users to elicit, analyse, and document functional and technical requirements
· Author User Requirement Specifications (URS) and Functional Requirement Specifications (FRS)
· Map common processes across manufacturing sites to enable Global PI design
Solution Design & Configuration
· Design site-specific and global Process Instructions (PIs) aligned to GMP requirements
· Configure Opcenter Execution Pharma / Simatic IT eBR modules end-to-end
· Collaborate with MES engineers on integration design with ERP, LIMS, and DCS/SCADA systems
Validation & Quality
· Lead validation activities in compliance with GxP, 21 CFR Part 11, and EU Annex 11
· Develop IQ/OQ/PQ test scripts, Design Specifications, and Traceability Matrices
· Support defect resolution and change management throughout delivery
Documentation
· Maintain comprehensive documentation: URS, FRS, Design Specs, Test Scripts, and SOPs
· Ensure all artefacts meet internal quality standards and client requirements
Team Leadership & Stakeholder Management
· Lead and mentor junior consultants; assign tasks and provide technical guidance
· Report project status, risks, and issues to Cognizant and client management
· Facilitate workshops, training, and knowledge transfer sessions
Job Requirements
Experience (Essential)
· Minimum 5 years of hands-on MES implementation experience, with strong expertise in Siemens Opcenter Execution Pharma (Simatic IT eBR) or equivalent pharma MES platform
· Proven delivery track record in pharmaceutical, biotech, or life sciences projects
· Solid exposure to GxP-regulated environments; working knowledge of 21 CFR Part 11, EU Annex 11, and GAMP 5
· Demonstrated ability to gather requirements and author functional specifications
· Experience leading or mentoring team members in a project setting
Technical Skills
· Strong proficiency in Opcenter Execution Pharma / Simatic IT eBR configuration and PI design
· Good understanding of MES integration patterns (ERP, LIMS, DCS/SCADA, historians)
· Familiarity with batch manufacturing, dispensing, packaging, and QC workflows
· Competency in validation methodology and documentation standards
· Working knowledge of SQL or data query tools is advantageous
Competencies
· Analytical mindset with structured problem-solving approach
· Excellent communication skills — effective with both technical and business audiences
· High attention to detail and commitment to quality outcomes
· Self-motivated; thrives independently and in collaborative team settings
Qualifications
· Degree in Engineering, Computer Science, IT, Pharmacy, or related discipline
· Opcenter / MES certifications are advantageous
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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
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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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