Master Data Associate

3 giorni fa

Latina, Italia Johnson & Johnson A tempo pieno

**About Innovative Medicine**

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

**We are searching for the best talent for**MASTER DATA ASSOCIATE**to be in**Borgo San Michele - Latina**

**Purpose**:
For the Italian Production Plant of Johnson & Johnson Innovative Medicine (Borgo San Michele - Latina) we are looking for a Master Data Associate to be hired for a permanent contract in the Data Readiness Department.

With the scope of increase the strategic vision of the Data Readiness organization, the “Master Data Associate” will be responsible for executing of base business activities related to sku conversions, enabling Latina site mission as a Launch & Growth site by keeping focus and alignment both on the creation of new Launch SKUs and the conversion of existing SKUs.

The person will be part of the Master Data team and will report to the Data Readiness Lead.

**You will be responsible for**:

- Executing base business activities respecting the procedures
- Guaranteeing steps execution in pipeline according to the planning date
- Ensuring to respect quality and compliance of the activities of whose will be responsible
- Collaborating with the stakeholders in terms of increase productivity/readiness of the base business in master data department
- Escalating issue according performance management (daily/weekly/monthly)
- Collaborating as Master Data contact point into the new Manufacturing Execution System team in order to give support for the implementation of the Master Batch Record inside Pas X language.

**Qualifications / Requirements**:

- Master’s degree in engineering, Farmacy, CTF, Chemistry or Economy is preferred
- Good knowledge of programming languages (e.g. Pas X and Library programming approach) is preferred.
- Good knowledge of material master / check list manager/sap.
- Good knowledge of quality, compliance and GMP related to manufacturing and packaging of pharmaceutical products.
- Ability to work in a cross functional team to ensure the correct execution of the activities according to the agreed timing and quality.
- Skills of ownership and accountability.
- Skilled in problem-solving and decision making.
- Experience in similar role is preferred.
- Good knowledge of English language (B2 level and above).

Li-Hybrid

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