Janssen Italy - Latina, Italia - Johnson & Johnson

Johnson & Johnson

Azienda verificata

Latina, Italia

1 settimana fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years.

The Latina site is the most innovative drug product (DP) manufacturing site in the Janssen pharmaceutical Johnson & Johnson Supply Chain Small Molecule Platform.

We ensure our life saving medicines reach the patient, safely, reliably, competitively, always.

As the DP Launch and Grow site for Small Molecule platform, the site is closely connected, with our R&D partners and with our API launch site in Geel, Belgium.

For the Italian production plant of Janssen (Borgo San Michele - Latina) we are looking for a
QC LS Scientist (Projects Supervisor) to be hired with a PERMANENT CONTRACT in the QUALITY CONTROL DEPARTMENT.

The person will lead the QC Lab Support group, composed of 6-8 directly reporting people, and will report to the QC Manager.

The focus area of the Lab Support group are:

Innovation projects proposal and implementation
Core business activities like shipments, management of consumables, data trending for NIR test, master data creation, etc

Main responsibilities:

Coordinate the activity of the QC Lab Support personnel in the following main focus area:

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Project management:

Build and develop the project team to ensure maximum performance, by providing purpose, direction, and motivation
Lead projects from requirements definition through deployment, identifying schedules, scopes, budget estimations, and implementation plans, including risk mitigation
Coordinate internal and external resources to ensure that projects adhere to scope, schedule, and budget
Analyze project status and, when needed, revise the scope, schedule, or budget to ensure that project requirements can be met
Establish and maintain relationships with relevant customers, providing daytoday contact on project status and changes

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Innovation:

Be in contact with the global Laboratory team to assess the new technologies and support the management to build a technology implementation roadmap in the QC
Ensure the digitalization process of the laboratory

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Base business activity coordination through the team members:

Stability:
Guarantee that the Stability Monitoring Program is addressed on yearly base according to the process relevant procedures
Support the Stability standardization processes influencing the global teams and bringing the voice of the site in the global platform

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Consumable management:

Guarantee the stock of consumables, reagent, and standards to avoid interruption of the analytical activities
Manage the expired reagents and their life cycle

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Laboratory electronic system master data management:

Empower (methods, reports, projects and custom field creation)

- iLAB

Smart QC
Checklyst manager

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Supporting activities for the lab:

Shipments
Document management (Periodic review, RMS and DR management)
Track and trending reports

The QC LS Scientist (Projects Supervisor) will be required to successfully address these activities with the following focuses:

Being part of the global network to guarantee the standardization of the processes and creating a network of global support
Ensure an efficient and dynamic organization able to support the business and focusing the group efforts to the customer satisfaction
Being a coach for the teammates
Ensure the adequacy of people, processes and performance through periodic evaluations and continuous monitoring to identify, in a timely manner, systematic gaps or potential situations of noncompliance.
Guarantee the adequacy of personnel, both internal and external, through periodic assessments and continuous monitoring, ensuring that training needs are systematically addressed.
Ensure the correct preservation of all records associated with the activities of the QC Lab Support.
Support the audit to the company for the area of competency
Ensure the presence of a prompt and effective communication and the presence of an escalation process to bring quality and performance issues at the appropriate level of management.
Ensure that the changes introduced in the organization, in the procedures and processes are managed so that all aspects concerning Safety, the Environment and Occupational Hygiene are evaluated and resolved.
Propose activities for the continuous improvement of the conditions of the areas of work, safety devices and behavior consistent with the company strategy.
Guarantee the professional development of collaborators.
Ensure the improvement of the quality of the working environment by promoting and encouraging actions consistent with the corporate Credo.

Qualifications: