QUALITY CONTROL SPECIALIST

Quality Control – QC Specialist & Coordinator, permanent contract 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.
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Are you passionate in Electronic Systems? Do you like to give structure to processes? Are you willing to Engineer and Standardize manifold processes that allow the laboratory to work flawless? Are you a curious person that wants to become expert of many topics? If these questions describe your aspiration, you can leave your personal mark in J&J applying for the position of QC Specialist (Supervisor Deputy) to be hired with PERMANENT CONTRACT in the QUALITY CONTROL DEPARTMENT for the Italian production plant of Johnson & Johnson (Borgo San Michele-Latina).
The person will be part of QC Lab Support (LS) group and will report to the QC Technology & Innovation Supervisor.
LS  group is responsible of.
          Innovation projects proposal and implementation (High Focus on automation/digitalization)  Core business activities like shipments, management of consumables, data trending for NIR test, master data creation, etc…   As a key member of our team the QC lab Support specialist will.
  ·       Coordinate the core business activities of QC Lab Support personnel in the following main focus area.
  o 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 o 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 o Laboratory electronic system master data management.
§  Empower (methods, reports, projects and custom field creation) §  iLAB §  Smart QC §  Checklyst manager o Supporting activities for the lab.
§  Shipments §  Document management (Periodic review, RMS and DR management) §  Track and trending reports §  Document review ·       Project management.
o Lead projects from requirements definition through deployment, identifying schedules, scopes, budget estimations, and implementation plans, including risk mitigation.
o Analyze project status and, when needed, revise the scope, schedule, or budget to ensure that project requirements can be met.
o Establish and maintain relationships with relevant customers, providing day-to-day contact on project status and changes.
  ·       Innovation.
o 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 o Ensure the digitalization process of the laboratory guaranteeing.
§  The Sustainability of the digital process put in place by the different project teams.
§  The continuous improvement of the digital workflows of the lab ensuring a reliable and smart master data management.
  ·       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.  ·       Apply and implement, where possible, Lean methodology aimed at simplifying processes and reduce steps of no added value.
·       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.
Qualifications Requirements/Skills and Qualifications.
·       Master Degree in CTF, Chemistry, Biology or Engineering or equivalent.
·       At least 3 years of working experience in related pharma environments.
·       Experience in an analytical laboratory is preferred.
·       Experiences on the shop floor and/or technical skills are appreciated.
·       Organizational skills are required.
·       Strong written and verbal communication skills.
·       Fluency in Italian is required.
·       Fluency in English is required.
Diversity, Equity & Inclusion at Johnson&Johnson means that “YOU belong”! For more than 130 years, diversity, equity & inclusion have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.