Quality Control Technician

6 giorni fa


Latina, Italia Johnson & Johnson Innovative Medicine A tempo pieno

Quality Control Technician – Johnson & Johnson Innovative Medicine – Location: Latina, Italy (12‑month fixed term at the Borgo San Michele production site). Overview We’re looking for the best talent for the role of Quality Control Technician, focused on ensuring product compliance with national and international pharmaceutical regulations, from product control to documentation. Responsibilities Execute, following training, standardised procedures and directives, all operations required for chemical, physicochemical and microbiological analysis using laboratory equipment. Ensure execution of analytic tests defined by programmes on raw materials, intermediates, finished products, stability of monitoring, experimental, environmental controls, cleaning validation, facility water, according to required timelines and high reliability standards, assessing conformance and validity of results. Use independently, according to standardised programmes, complex equipment and instruments; use data processing units. Perform laboratory tests correctly through study of fundamental principles, applied theory and good laboratory practices (GLP), develop numerical calculations during data processing, proposing ideas and suggestions based on observations and conclusions. Ensure recording of all data related to methodologies, observations and conclusions of analyses, using, when necessary, computer tools. Guarantee integrity of data at all times. As part of the training package, participate in practical laboratory management, including instrumental maintenance, drafting/ revising procedures or protocols, tuning and validating analytical methods for new products and adjusting existing ones, producing necessary documentation. Ideal Profile (Qualifications) Diploma/Degree in scientific disciplines and >6 months of experience as a laboratory technician in the pharmaceutical field (both chemical and microbiological). Excellent knowledge of GMP regulations, use of eLIMS, Empower 3, SAP. Consolidated experience in HPLC–UPLC (identifications, titres, degradates) and rapid qualitative‑quantitative analyses via NIR, pH, conductivity, Karl Fisher, TOC, microbiological analyses. Intermediary level English language proficiency. Excellent knowledge of Data Integrity requirements. Strong teamwork skills, cooperative attitude, respect for high safety standards, ability to manage and communicate critical issues during laboratory activities, meet deadlines, tenacity in achieving goals. What You Can Expect Application review: We’ll carefully review your CV to see how your skills and experiences align with the role. Getting to know you: If there’s a good match, you’ll be invited to a short call with a recruitment team member. Staying informed: Recruitment team updates you at each step. Final steps: Successful candidates will complete country‑specific checks before starting the role. Preferred Skills Administrative Support, Agility Jumps, Communication, Compliance Management, Customer Centricity, Document Management, Execution Focus, Factory Acceptance Test (FAT), Persistence and Tenacity, Process Oriented, Quality Control (QC), Quality Standards, Quality Systems Documentation, Quality Validation, Teamwork. Seniority level Not Applicable Employment type Full‑time Job function Quality Assurance Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Johnson & Johnson Innovative Medicine by 2x. #J-18808-Ljbffr



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