MTO MES Modelling Specialist

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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MTO MES Modelling Specialist

Summary

Johnson and Johnson is recruiting for an MES Modelling Specialist! This position can be located at a Johnson and Johnson Innovative Medicine site in Cork, Ireland; Leiden, Netherlands; Schaffhausen, Switzerland; Latina, Italy; Geel, Belgium; Beerse, Belgium; Titusville, NJ; Gurabo, Puerto Rico, Wilson, NC.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at https://www.jnj.com

The MES Modelling Specialist plays a key role in supporting the standardized deployment of MES batch records across the MTO organization, as part of the NGM (Next Gen MES) Program. The MES Specialist will be part of a team of experienced Subject Matter Experts on batch record modelling, automation integration, business standardization and quality best practices. He or she supports initiation and acceleration of the deployment of global MES projects at site level enabling successful handover to the local project team.

The MES Modelling Specialist fosters collaboration across local sites, global, and technical teams to ensure seamless delivery and value realisation, while maintaining compliance and best practices.

Key Responsibilities

• Lead by example and strive to perform to high standards at all times in compliance with Credo and Standards of Leadership. Act as a role model for all colleagues within the Deployment Excellence team.

• Support the execution of NGM projects across MTO.

• Business relationship management and ensuring the NGM program and best practices are meeting business requirements.

• Provision of suitable training courses and training material

• Define SOPs for NGM enabling services

• Assure the safe execution of job activities and follow good environmental practices and procedures.

• Ensure that personal training requirements are completed in compliance with site procedures.

• Ensure that NGM documentation is managed, controlled, approved and reviewed in accordance with global procedures.

• Develop and monitor Department metrics/KPIs to ensure that departmental goals and targets are met.

• Drive efficiencies across the NGM program and site through suitable adoption of new technologies and enhanced approaches to how we operate (Challenge the Status Quo and drive improvement).

• Working with BPO and TPO leads to solicit and deploy technologies, systems and sharing to improve globally.

Experience, Skills, and Qualifications

Required:

• Third level Degree in engineering, science or an IT discipline.

• Five years plus of modelling experience within a pharmaceutical or GMP regulated manufacturing environment.

Preferred:

• Technical knowledge of S95 Level 3 Electronic Batch systems such as Werum MES PAS-X.

• Good understanding of S95 level 4 systems and their capabilities such as ERP, Quality Systems, Data warehouses etc., to facilitate the transition to integrated Systems within the batch record.

• Strong process knowledge for Drug Substance or Drug Product Manufacturing.

• Understanding of the ISA S95 & S88 standards and how they should be used within the Global Supply Chain

• Good appreciation of Industry 4.0/IIoT and how we can effectively drive to transform within this framework.

Other Requirements

• Good appreciation of Industry 4.0/IIoT and how we can effectively drive to transform within this framework.

Key Skills:

• Customer focused and results driven

• Excellent verbal and written communication skills

• Innovative

• Good problem solving skills

• Collaboration and teamwork across site functions and other JSC / J&J sites

• Demonstrate Integrity and Credo-based actions at all times

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com .

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