PpFAMAR is a European contract manufacturing and development partner, for the pharmaceutical and health beauty industry. Building on over 75 years’ expertise, we deliver flexible solutions, from development to production and distribution. Driven by our customer-care mindset, we offer services covering the majority of pharmaceutical forms. Through the outstanding knowledge and commitment of our 1850 employees and with a network of 7 production sites, we supply a wide range of 1800 products in 125 international markets. /p pFor our Italian plant in Baranzate (MI), which specialises in the production of oral solids, we are looking for an experienced and qualified professional to fill the position of Manufacturing Department Manager within the Production, Pharma Maintenance Transfer department, reporting directly to the Head of Production. /p pThis role is responsible for leading operations within our Solid Oral Dosage Forms department, ensuring the efficient, compliant, high-quality and timely production of tablets, capsules, and other solid oral pharmaceutical products, as well as overseeing the successful transfer of new products into manufacturing. /p h3KEY RESPONSIBILITIES /h3 ul liOversee daily manufacturing activities for solid oral dosage forms, ensuring adherence to GMP and regulatory standards /li liLead and manage a team of shift supervisors and MFG operators to meet production targets /li liCollaborate with Quality Assurance, Engineering, Maintenance, and Supply Chain to optimize processes and resolve operational issues /li liCollaborate with EHS to ensure full-compliance of Safety standard in the department, acting as the appointed Safety Supervisor (Preposto) for the area /li liMonitor KPIs such as yield, efficiency, downtime, and quality deviations; implement corrective actions as needed /li liEnsure accurate and compliant documentation (MBR) produced by the manufacturing department and manage all related ERP transactions for finished product delivery /li liDrive continuous improvement initiatives and ensure their effective implementation /li liEnsure proper training and professional development of team members /li liParticipate in audits and inspections by clients and regulatory authorities /li liManage departmental capacity planning and resource allocation /li /ul h3BACKGROUND REQUIREMENTS /h3 ul liUniversity Degree in CTF, Chemistry, Engineering, or a related field /li liMinimum 5 years of experience in pharmaceutical manufacturing, with at least 2 years in a leadership role. /li liStrong knowledge of GMP, AIFA, EMA, and other relevant regulatory guidelines. /li liProven experience with solid oral dosage technologies (granulation, compression, coating, encapsulation). /li liExcellent leadership, communication, and problem-solving skills /li liFluent in English /li /ul /p #J-18808-Ljbffr