Production Supervisor

for the site Borgo San Michele LT, Italy

Would you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you! Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs.

• To grant the correct execution of the department Tiers.
• To verify the feasibility of mid-term production plans with respect to available resources and market priorities. Also, to share any differences with the manager of the unit.
• Coordination with the Technical Assistance Unit, in order to grant the correct action time on the machines and reduce downtime.
• To support the section manager and the colleagues involved, in reviewing operational procedures, “DVR” and budget plans.
• To suggest innovative solutions to improve productive processes and reduce costs.
• Constantly and regularly, to communicate with the operational personnel with the aim to transfer information and respond to necessities or suggestions of improvement.
• To ensure that personnel respects EHS and GMP regulations.
• To participate actively as SME to regulatory and customer inspections.
• To assure the opening of deviations in case of anomalies compared to flows and processes.
• To promote/participate to the definition of change plan and CAPA plan for the own area of competence.
• Participate proactively to projects that impact on the own area of competence taking part on team projects.
• Ensure that the documentation for Batch Record (supporting validation protocols) is implemented correctly and delivered within the set time frame.
• To define training plan for employees and guarantee that the personnel is trained on procedures and that have the technical education of the various work centre to which it is assigned.
• To ensure the definition of standard of machine and labour hour for the products of own areas of competence according with the section manager.

• University degree in technical subjects preferred (Engineering, Chemistry, Pharmaceutical Chemistry, etc.).
• 3-5 years of People management experience.
• Good knowledge of GMP.
• Good knowledge of Oral Solid Dosage form.
• Good knowledge of English both written and spoken.
• Excellent knowledge of Office.
• Good knowledge of SAP system.
• Lean Six Sigma certification is a plus.
• Strong analytical approach with a high level of accuracy and attention to detail.
• Strong problem-solving and organizational skills.
• Ability to manage multiple priorities and work effectively under tight deadlines.
• Proactive mindset with a continuous improvement approach.

Are you looking for new challenges in a highly competitive environment? And you want to tackle them creatively and on your own responsibility? Do you prefer a "get-it-done" culture and think in terms of solutions rather than problems? What are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!