Janssen Italy - Qc Lab Support Scientist Supervisor LATINA

Janssen Italy - Qc Lab Support Scientist Supervisor
Latina
Lazio, LATINA

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 Lab Support Scientist Supervisor** to be hired with a PERMANENT CONTRACT in the QUALITY CONTROL DEPARTMENT.

The person will be responsible for leading the QC Lab Support group, composed of 6 directly reporting people, and will report to the QC Manager.

**Main responsibilities**:

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

- **Innovation projects**:

- Be in contact with the global Laboratory team to assess the new technologies and support the management to create a technology implementation roadmap in the QC

- Ensure the digitalization process of the laboratory

- Ensure the execution and completion of project-related activities in the QC area by the coordination of dedicated resources and / or through direct participation focusing in process performance improvement, cost reduction and process quality&compliance increase

- **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

- **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

- **Laboratory electronic system master data management**:

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

- iLAB

- Smart QC

- Checklyst manager

- **Supporting activities for the lab**:

- Shipments

- Document management (Periodic review, RMS and DR management)

- Track and trending reports

The QC LS Scientist 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 non-compliance

- 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 work activities within the area of competence they take place in accordance with current legislation on safety, Environment and Work Hygiene than J&J standards

- 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

- Master's Degree in CTF, Chemistry, Biology or Engineering or equivalent

- At least 5 years of working experience in related pharma environments

- Experience in an analytical laboratory is preferred

- Proven project management skills are required

- Experiences on the shop floor and/or technical skills are appreciated

- Communication, collaboration, data management and organizational skills are required

- Fluency in Italian is required

- Fluency in English is required

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 and will not be discriminated against on the basis of diversity.

**Primary Locatio