Master Batch Record & BOM Technician
Pubblicato il 09-08-2026 - Grafton Recruitment in Lazio
Grafton LifeScience* is a dedicated team focused on enhancing the experiences, skills, and potential of candidates in Sales & Marketing, Clinical Research, Regulatory, and Operations within the Pharmaceutical and Medical sectors. We also specialize in roles related to customer support in the health-impacting distribution field (Pharmacies and Parapharmacies).We are a team of passionate professionals working to guide our candidates towards roles and corporate environments that best match their skills and expectations. In partnership with an integrated CDMO with around 60 locations worldwide, specializing in integrated sterile liquid and lyophilized product development and commercial manufacturing, we offer an opportunity for Master Batch Record & BOM Technician : The main function of a Master Batch Record & BOM Technician is to draft, review, and manage manufacturing documentation and production master data, including base bills of materials and items, within the company information system.
This role ensures compliance with quality standards and regulatory requirements through collaboration with cross-functional teams. Ensure feasibility and operational application of instructions in Master Batch Records in collaboration with Production and Quality Specialists.
Draft initial Master Batch Records with Technology Transfer and Cleaning & Process Validation groups and manage them in the company system.
Review and formally approve initial drafts of Master Batch Records. Finalize and manage Master Batch Records in the company information system.
Approve Master Batch
Records by activating relevant personnel in compliance with standards, regulations, and customer instructions. Train production personnel on Master Batch Records. Manage change control in collaboration with other departments.
Manage changes in secondary packaging materials with Logistics and QA Packaging Development. Participate in technical meetings with clients for new process/product introductions or reviews. Manage customer requests in collaboration with other functions.
Relevant degree or proven experience in similar roles.
Experience in drafting and managing manufacturing documentation in a pharmaceutical or similar environment. Effective collaboration and communication skills.
Proficiency in English is desirable Contract Offer: Fixed-term agency contract from 07/09/2026 to 06/03/2027. CCNL Chimico-Farmaceutico, level D1-C2 Working time weekly: daily, Monday-Friday, (1 day smartworking) 198/2006 and subsequent amendments, as well as Legislative Decrees No.