Work Your Magic with us!  

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 

Education Qualification:

Bachelor’s degree in Science or Engineering related to IT\\Computer Science\\Electronics\\Instrumentation\\Pharmacy

Professional Experience & Responsibilities:

Minimum experience of 8+ years on MES PAS-X application V3.1.8, V3.2.7 and V3.3.2.Having a good hold on MES PAS-X Master Data Parameterization (Equipment Management, User Management, Rights Management, Control Data, Terminal Management, Printing/Reporting, Profiles, Production Units, WMS Master Data, and Service configuration.Having good knowledge of PAS-X functionality like weighing & dispensing module, equipment management, MBR design, and EBR and materials management/warehouse functionalityKnows MES integration with Level 2, Level 3, and Level 4 systems like SAP ERP, OSI PI, LIMS, Kepware OPCShould know about System Administration activities like User/Terminal/Printer management/System configuration and Scales configuration.Knowing Linux OS, Dockers, K8s, and PostgreSQL is an added advantage.Installation of Hotfixes, and service packs and ensuring the installation of Windows/Linux patches on the servers and mitigating vulnerabilities timely manner.Proven track record of leading, driving, and successfully closing IT projects in a complex, global matrix organization and proven ability to lead teams.As a Senior resource for MES PAS-X, you will be responsible for the delivery of the MES projects and Service Delivery Operations of MES.Responsible for 2nd level Support to the Business on MES.You should also be able to act proactively to ensure smooth team operations and effective collaboration.Familiar with current manufacturing models and concepts in Life Science and Healthcare and proven track record in Pharmaceutical GxP project implementation and validationUnderstanding of ISA88 and ISA95 standardsKnowledge of Computer Systems Validation, SDLC methodologies, 21CFR part 11, and cGMP including GAMP and EU Annex 11Have experience on new implementation and upgrade projects from requirement gathering stage to qualification and final delivery of MESShould be able to handle support tools like IT4YOU, HPSM and manage the delivery of various services like Incident Management, Problem Management, Change and Release management, etc.Experience on Databases like Oracle and Microsoft SQL servers is an advantage.Formal qualifications in PMP and ITIL are a plus.Excellent communication and leadership skills

 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!