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.
Job Responsibilities
- 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.
- Archive documentation for the established retention period.
- Manage changes in secondary packaging materials with Logistics and QA Packaging Development.
- Verify and monitor procedure application to ensure compliance with quality standards.
- Collaborate with Quality Specialists in their activities.
- Participate in technical meetings with clients for new process/product introductions or reviews.
- Manage customer requests in collaboration with other functions.
- Support Quality in managing deviations, complaints, investigations, and corrective actions.
Do you have these skills and requirements?
- 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.
- Attention to detail and organizational abilities.
- Ability to manage documentation workflows and change control processes.
- 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)
Place of work: Ferentino (FR)
Grafton LifeScience is a specialization of Gi Group Spa authorized to operate by the Ministry of Labor and Social Policies (Authorization No. 26/11/2004 PROT. 1101 - SG).
The offer is intended for candidates in compliance with Legislative Decree No. 198/2006 and subsequent amendments, as well as Legislative Decrees No. 215 and No. 216 of 2003 on equal treatment.
Candidates are invited to read the privacy notice pursuant to Articles 13 and 14 of EU Regulation 679/2016 at the following address: "