Manager SCO-Manufacturing

Full Job Description

The opportunity

This is a rapidly growing area, so you will have plenty of opportunity to spread your wings and develop your skillset to keep up with the ever-growing demands of the digital landscape. Most of your time will be spent embedded with our clients’ team and we’ll look to you to provide our clients with a unique business perspective on how they must continue to innovate and remain competitive in this ever-changing industry. You should be willing to support the US, EU and other onsite teams as per their time convenience(though not always). High degree of flexibility desirable. You may need to travel onsite at the go to study client processes and come out with solutions quick fixes.

Job Summary: We are seeking an experienced Digital Manufacturing Project Manager to lead end-to-end implementation of digital transformation projects with strong background in Manufacturing Execution Systems (MES), Internet of Things (IoT), and Industrial Automation within the pharmaceutical sector.

Skills

Qualifications:

• Should have 10 - 12 years of experience in project management, with a strong focus on digital manufacturing MES and Industrial Automation specifically in pharmaceutical industry.
• Should have been experienced in end-to-end implementation of any Pharma MES. In addition, Hands-on experience working on Rockwell FTPC, Werum PAS-X, SAP Manufacturing Execution System, Siemens MES would be added advantage.
• Should collaborate with IT and other departments to ensure seamless integration of MES with ERP, LIMS, and other enterprise systems within the pharmaceutical industry.
• Knowledge of software/systems technologies associated with integration and customization of MES solutions including Microsoft .NET, HTML, Visual Basic, SQL would be added advantage.
• Identify new opportunities for process optimization and enhancements within the Pharma MES framework. Also, responsible to identify project risks and develop strategies for mitigation, ensuring that potential obstacles are addressed before they impact project timelines.
• Good knowledge on understanding new project scope, objectives, and deliverables in collaboration with stakeholders, creating detailed project plans that outline timelines and resource requirements.
• Ensure to adhere pharmaceutical industry compliance and regulations such as FDA 21 CFR Part 11 and Good Manufacturing Practices (GMP).
• Establish and monitor Pharma related key performance indicators (KPIs) to assess project effectiveness and drive continuous improvement initiatives.
• Management related certifications such as Project Management Professional (PMP) certification or similar credentials are additional advantage.

What working at EY offers

EY is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment.\n\nAll employment decisions here are based on business needs, job requirements and individual qualifications, without regard to age, race, colour, religion, sex, national origin, disability, or any other legally protected basis, in accordance with applicable law in the locations where we operate.\n\nDiversity, inclusiveness and respect for all employees form the basis of our culture and are essential to our success. We value each individual’s distinct contribution and leverages the collective strengths to ensure that we contribute in building a better working world.