Job Summary
Serve as a senior consultant driving design and implementation of manufacturing execution and digital transformation solutions for global pharma manufacturing clients using strong expertise in MES platforms industry 4.0 concepts and manufacturing processes to improve quality compliance efficiency and data driven decision making in a hybrid work environment with day shift schedule.
Responsibilities
- Lead complex consulting engagements for pharma manufacturing clients by assessing current MES and shop floor capabilities and defining clear transformation roadmaps that align with business goals and regulatory expectations.
- Develop robust MES solution designs that integrate production quality and warehouse processes to deliver real time visibility traceability and electronic batch records tailored to pharma manufacturing needs.
- Coordinate detailed requirement gathering workshops with cross functional client stakeholders to capture user journeys system interactions and compliance constraints that influence MES and industry 4.0 solutions.
- Configure and guide implementation of MES functionalities such as work order management recipe execution deviation capture and equipment integration to optimize manufacturing cycle times and reduce errors.
- Drive integration between MES laboratory systems enterprise planning and equipment control systems to create a connected manufacturing landscape that supports industry 4.0 use cases.
- Analyze production data from MES and related digital platforms to identify patterns inefficiencies and improvement opportunities and translate findings into actionable optimization plans.
- Prepare clear functional specifications configuration documents and test scenarios that ensure traceable alignment from business requirements through validation and go live.
- Collaborate with validation teams to support computer system validation activities for MES deployments so that all documentation testing evidence and traceability meet pharma regulatory standards.
- Guide incident resolution problem analysis and continuous improvement activities for live MES environments to maintain high system availability and stable operations.
- Mentor junior consultants and project team members by sharing best practices in MES design pharma manufacturing processes and digital manufacturing concepts to build overall team capability.
- Coordinate with product vendors and internal architecture teams to evaluate new industry 4.0 technologies such as advanced analytics digital twins and smart devices and assess fit for client environments.
- Communicate project status risks and mitigation actions to client stakeholders in a structured manner that enables timely decisions and maintains alignment with project objectives.
- Participate in business development activities by contributing to solution proposals effort estimates and demonstrations that showcase MES and industry 4.0 capabilities.
Qualifications
- Describe extensive experience in implementing MES solutions within pharma manufacturing environments and applying industry 4.0 principles to enhance operational excellence.
- Demonstrate strong understanding of manufacturing and supply chain processes including production planning materials management quality operations and warehouse workflows.
- Exhibit familiarity with regulatory frameworks relevant to pharma manufacturing such as good manufacturing practice and validation expectations for computerized systems.
- Apply knowledge of systems integration concepts to connect MES with enterprise resource planning quality systems and shop floor control equipment using standard integration patterns.
- Utilize strong consulting skills including stakeholder management requirement analysis documentation and user training to ensure successful adoption of MES and digital solutions.
- Show capability to work effectively in a hybrid model and coordinate across global teams while maintaining clear communication and timely delivery in a day shift context.
Certifications Required
Preferred certifications include MES platform certification and industry 4.0 or smart manufacturing professional credential.
Things to know before you apply
- Work authorization: Cognizant will only consider applicants for this position who are legally authorized to work in Canada without requiring employer sponsorship, now or at any time in the future.
- Accommodations: If you have a disability that requires reasonable accommodation to search for a job opening or submit an application, please email [email protected] with your request and contact information.
- AI in hiring: We use artificial intelligence (AI) tools to help us screen and assess applications more efficiently. Our team performs additional human review and ultimately decides who moves forward in our hiring process.
- Open position: Unless otherwise stated, this job posting is for an open position on our team.
- Language proficiency: We ask that all candidates have basic English proficiency for company-wide communications purposes. For roles based in Quebec, professional English proficiency is required, as you’ll deliver services to and collaborate with stakeholders outside the province who may not speak French.
- Inclusion: Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, provincial or local laws.
About Cognizant
Cognizant (Nasdaq: CTSH) is an AI Builder and technology services provider, bridging the gap between AI investment and enterprise value by building full-stack AI solutions for our clients. Our deep industry, process and engineering expertise enables us to build an organization’s unique context into technology systems that amplify human potential, drive tangible outcomes and keep global enterprises ahead in a fast-changing world. See how at cognizant.ai or @cognizant.











