Mes Implementation Coordinator - Parma, Italia - GSK

GSK

Azienda verificata

Parma, Italia

3 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

Site Name:
Italy - Parma

Posted Date:
May

MES Implementation Coordinator (e-brs)

The purpose of this role is to lead and facilitate the implementation of manufacturing execution systems, in the manufacturing, inspection and packaging areas of Parma site, including but not exclusively eBRS, ePEL, AWD.

For their allocated project and scope, they act as a single point of accountability for the site and above site teams.

This role requires a balance of the following skills:

Business process change management
Project management via leadership of cross functional teams and stakeholder management
Technical breadth with agility to drive efficiency and improvements across the site
Ability to deliver a right firsttime solution ontime and within budget.

In this role, you will

Be accountable to implement the solution agreed with the impacted stakeholders to time, cost and quality to achieve the agreed benefits/business result.
Work with the central teams to identify suitable solutions for site MES requirements, acting as primary point of contact for that solution at site and participating in the relevant Community of Practices
Work with the operations managers and the quality functions to elaborate the business requirements and impact of adopting central standards. Challenge local teams to simplify and improve business processes being digitalized (continuous improvement mindset on quality/safety/productivity/analytics readiness).
Manage project and business change plan, assuring that site resources/implementation activities are compatible with the production program, and that activities of vendors/automation team are aligned to implementation plan.
Manage the project costs and cross charges Maintain regular communications with stakeholders on progress, risks, issues, successes, and escalations.
Coordinate the site governance and decisionmaking process.
Be responsible for Role Mapping, Training and Learning plan, Communication plan. Supports the UAT and PQ design and execution by the site team.
Ensure robust support model defined and handover from project to BAU is completed in a audit ready way.
Be responsible for ensuring that Risk assessment, Risk communication and action planning are completed in accordance with our Risk Management System (RMS) within the relevant business area. Risks may be relevant to Business, Business continuity, Safety, People, Wellbeing, Compliance, Quality, Costs.

Basic Qualifications & Skills:

Master's Degree in Technical/Scientifical discipline
Experience in managing projects dedicated to the GMP documentation
Continuous Improvement Mindset (Safety, Quality, Service, Cost, Future Ready)
Knowledge of English language

Preferred Qualifications & Skills:

5+years in a pharma environment with experience in managing complex GMP records and related deviations
Knowledge of the main technologies that can be used to improve learning
Knowledge of IT solutions useful for digital transformation.
Negotiation skills and ability to guide local project teams and communicate with the Above Site project team

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive.

Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutely depends on our people.

While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive.

We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy.

We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

GSK is an Equal Opportunity/Affirmative Action Employer.

All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

Important notice to Employment businesses/ Agencies

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.

This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state U